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Pharmaceutical Ingredients
Cetirizine Di Hydrochloride
Minimum Order Quantity: 50 Kg
Product Brochure
| Grade Standard | BP |
| Certification | BP, USP, EP, IP |
| Grade | Pharma grade |
| Purity | 99% |
| Physical State | Powder |
| Packaging Size | 25 kg |
| Packaging Type | HDPE Bags |
| Color | White |
| Molar mass | 388.89 g/mol |
| Formula | C21H25ClN2O3 |
Cetirizine Dihydrochloride API Powder – Active Pharmaceutical Ingredient
Product Name: 2‑Chloro BHP Cetirizine / Cetirizine Dihydrochloride
CAS Number: 83881-52-1
Synonyms: Cetirizine HCl; 2-[4-[(4-Chlorophenyl)phenylmethyl]-1-piperazinyl]ethoxy]acetic acid dihydrochloride
Molecular Formula: C₂₁H₂₅ClN₂O₃·2HCl
Molecular Weight: ~461.81 g/mol
Appearance: White to off-white crystalline powder
Grade: IP / BP / USP / Pharmaceutical Grade
Purity: Typically ≥ 98 % assay (HPLC / Pharmacopoeial standard).
Description:
Cetirizine Dihydrochloride is a second-generation antihistamine API widely used in the pharmaceutical industry for the formulation of anti-allergy medications. As a highly selective H₁ histamine receptor antagonist, it helps manage and relieve symptoms of allergic conditions such as allergic rhinitis (hay fever), urticaria (hives), dermatitis, and other hypersensitivity reactions.
Key Features & Properties:
CAS No: 83881-52-1
Chemical Name: Cetirizine dihydrochloride, antihistaminic agent
Appearance: White to off-white crystalline powder
Purity: ≥ 98 % (pharmaceutical grade, assay by HPLC/titration)
Solubility: Soluble in water and methanol; practically insoluble in non-polar solvents.
Melting Point: ~205 – 225 °C range (pharmacopoeial typical)
Pharmacological Action: Peripherally selective antihistamine with minimal central sedation compared to first-generation antihistamines.
Hygroscopicity: Slightly hygroscopic crystalline form.
Applications:
Cetirizine Dihydrochloride API Powder is mainly used in the manufacture of pharmaceutical formulations, such as:
Oral tablets and capsules.
Syrups and suspensions.
Chewable tablets.
Pediatric formulations.
Antihistamine combinations and multi-ingredient allergy products.
It is essential for anti-allergy and antihistamine drug products designed to relieve symptoms of allergic rhinitis, hay fever, urticaria, and other allergic conditions.
Typical Packaging:
25 kg / 50 kg HDPE drums with protective lining.
Fiberboard drums or cartons.
Custom export-grade packaging available on request.
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Tenoxicam Chemical IP/BP/USP/EP
Product Brochure
| Molar Mass | 337.376 g/mol |
| ChemSpider ID | 4471584 |
| Elimination Half Life | 30-140 hours |
| ATC Code | M01AC02 (WHO) |
| PubChem CID | 5282194 |
| Grade Standard | IP/BP/USP/EP |
Product Name: Tenoxicam API PowderSynonyms: 4‑Hydroxy‑2‑methyl‑N‑(pyridin‑2‑yl)‑2H‑thieno[2,3‑e][1,2]thiazine‑3‑carboxamide 1,1‑dioxideCAS No.: 59804‑37‑4.Grade: Pharmaceutical‑Grade API (IP / BP / USP / EP compliant).
Product Overview:
Tenoxicam API Powder is a high‑quality active pharmaceutical ingredient (API) belonging to the non‑steroidal anti‑inflammatory drug (NSAID) class. It is widely used as a raw material in the formulation of anti‑inflammatory, analgesic, and antipyretic pharmaceuticals. Its therapeutic effects include relief from pain, inflammation, and stiffness associated with conditions such as osteoarthritis, rheumatoid arthritis, ankylosing spondylitis, acute musculoskeletal pain, and other inflammatory disorders.
Chemical & Physical Properties:Chemical Name: 4‑Hydroxy‑2‑methyl‑N‑(pyridin‑2‑yl)‑2H‑thieno[2,3‑e][1,2]thiazine‑3‑carboxamide 1,1‑dioxide Molecular Formula: C₁₃H₁₁N₃O₄S₂ Molecular Weight: ≈337.37 g/mol Appearance: White to yellow crystalline powder Purity: Typically ≥98 % (HPLC) pharmaceutical grade. Solubility: Practically insoluble in water; slightly soluble in organic solvents; may be micronized for improved dissolution during formulation. Melting Point: ~209–213 °C (decomposition). Storage: Cool, dry place; protect from light and moisture.
Key Features & Benefits:Pharmaceutical‑grade API suitable for finished drug formulations. High purity and consistent quality with documentation such as COA and MSDS available on request. Potent analgesic and anti‑inflammatory activity, ideal for NSAID formulations. Stable crystalline powder for ease of handling, storage, and processing. Compliant with global pharmacopeial standards (IP/BP/USP/EP where applicable).
Usage & Handling:For pharmaceutical manufacturing and research use only — not for direct ingestion in raw form.Handle with appropriate PPE (gloves, mask, goggles).Store in a cool, dry, ventilated area, protected from moisture and direct sunlight.Follow all applicable regulatory, safety, and compliance standards for APIs.
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Isopropyl Chloro Acetate API
Product Brochure
| CAS Number | 105-48-6 |
| Linear Formula | ClCH2CO2CH(CH3)2 |
| Molecular Weight | 136.58 g/mol |
| EC Number | 203-301-7 |
| MDL Number | MFCD00040410 |
Product Name: Isopropyl Chloroacetate (IPCA) API PowderCAS No.: 1642-95-3Purity: ≥99% (or specify grade)Form: White to Off-White Crystalline PowderGrade: Industrial / Technical / Pharma Intermediate.
Product Overview:
Isopropyl Chloroacetate (IPCA) is a high-purity chemical intermediate widely used in organic synthesis and pharmaceutical manufacturing. Known for its excellent reactivity and stability, IPCA plays a key role in the synthesis of active pharmaceutical ingredients (APIs), agrochemicals, fragrances, and specialty chemicals.
Key Features & Benefits:High Purity: Manufactured under controlled conditions for consistent quality.Stable & Reliable: Minimal impurities ensure dependable performance in chemical reactions.Versatile Intermediate: Suitable for various organic synthesis and formulation applications.Good Solubility: Easily soluble in many organic solvents aiding smooth processing.Quality-Assured: Tested for appearance, purity, and performance parameters.
Packaging Options:1 kg / 5 kg / 25 kg HDPE Drums.Custom Packaging available on request.
Safety & Handling:Store in a cool, dry place, in a tightly closed container. Handle in accordance with recommended safety practices.
Why Choose Us:Trusted Supplier with consistent quality.Competitive pricing and bulk availability.Prompt delivery and responsive customer support.Customization and technical support available.
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Trimethyl Sulfoxonium Iodide API Powder
Minimum Order Quantity: 25 Kg
Product Brochure
| Physical State | Powder |
| Form | Powder |
| CAS Number | 1774-47-6 |
| Melting Point | 208 to 212 deg C (406 to 414 deg F; 481 to 485 K) |
| PubChem CID | 74498 |
| Molar Mass | 220.07 g.mol-1 |
| Chemical Formula | C3H9IOS |
| Purity | 99% |
Product Name: Trimethyl Sulfoxonium IodideSynonyms: TMSI, Trimethylsulfoxonium iodide, (CH₃O)₃S⁺I⁻CAS Number: 3338-39-6Molecular Formula: (CH₃O)₃S.IMolecular Weight: 211.2 g/mol
Description:
Trimethyl Sulfoxonium Iodide is a high-purity, white to off-white crystalline powder that serves as a potent intermediate in organic synthesis. It is commonly used in pharmaceutical and chemical industries for its ability to introduce sulfonium groups into organic molecules. This compound is widely employed in the production of various complex molecules, such as in the synthesis of chiral compounds and as a reagent in organic reactions like nucleophilic substitution.
Key Features & Benefits:High Purity API Grade: Manufactured under strict quality control to meet industry standards for pharmaceutical use.Versatile Reagent: Highly effective in organic synthesis, particularly in the formation of sulfonium salts and in nucleophilic substitution reactions.Stable & Efficient: Provides excellent stability and ease of handling in various chemical processes.Widely Used in Pharmaceuticals: Ideal for the synthesis of specialty chemicals, chiral intermediates, and active pharmaceutical ingredients (APIs).Chemical Compatibility: Works well in combination with other reagents in organic chemistry, making it a versatile choice for lab and industrial-scale reactions.
Typical Specifications (Indicative):Appearance: White to off-white crystalline powder.Purity: ≥98% (meets API specifications)Molecular Weight: 211.2 g/molMelting Point: ~140°C (range).Solubility: Soluble in water and organic solvents like acetone, methanol, and ethanol.Identification: Matches the IR spectrum of Trimethyl Sulfoxonium Iodide.
Packaging Options:25 g / 50 g / 100 g bottles.1 kg / 5 kg drums (Custom packaging options available).Bulk supply for contract manufacturing and API production.
Storage and Handling:Store in a cool, dry place in a tightly sealed container. Avoid exposure to moisture or air. Handle with appropriate protective equipment such as gloves, goggles, and lab coat to ensure safety during handling.
Why Choose Our Trimethyl Sulfoxonium Iodide Powder?We supply high-quality Trimethyl Sulfoxonium Iodide with consistent purity and reliable performance, suitable for both small-scale research and industrial applications. Our product ensures enhanced synthesis efficiency and superior chemical reactivity, backed by our commitment to timely delivery, competitive pricing, and customized packaging solutions.
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Lidocaine Hydrochloride API
Product Brochure
| Grade Standard | Technical |
| Packaging Type | HDPE Bags |
| Packaging Size | 25 kg |
| Purity | 98% |
| Manufacturer | Remedy Labs |
| Form | Powder |
| Molar Mass | 234.34 g/mol |
| Application | Industrial |
| Formula | C14H22N2O |
Lidocaine Hydrochloride API
Product Name: Lidocaine Hydrochloride API
Synonyms: Lignocaine Hydrochloride, Lidocaine HCl, Xylocaine Hydrochloride, 2‑(Diethylamino)‑N‑(2,6‑dimethylphenyl)acetamide Hydrochloride
CAS No.: 73‑78‑9
Molecular Formula: C₁₄H₂₂N₂O · HCl
Molecular Weight: 270.80 g/mol
Appearance: White to off‑white crystalline powder.
Grade: Pharmaceutical / API (IP / BP / USP / EP).
Product Description:
Lidocaine Hydrochloride API is a high‑purity active pharmaceutical ingredient widely used in the global pharmaceutical industry as a local anesthetic and antiarrhythmic agent. It is supplied as a free‑flowing white crystalline powder manufactured to conform with major pharmacopoeial standards such as IP, BP, USP and EP, making it ideal for formulation into a variety of medical products.
Lidocaine Hydrochloride works by blocking sodium ion channels in nerve membranes, inhibiting nerve impulse conduction and producing effective local or regional anesthesia. It has a rapid onset and intermediate duration of action, which makes it a versatile choice for medical, dental and minor surgical procedures. Additionally, its antiarrhythmic properties enable its use in cardiac care.
Key Features:
Pharma‑grade API: Conforms to IP/BP/USP/EP specifications for pharmaceutical use.
High purity: Typically ≥98 % assay, ensuring consistent performance in formulations.
White crystalline powder: Easy to handle and process in manufacturing.
Soluble: Readily soluble in water and alcohol, facilitating formulation into solutions, gels, creams and injectables.
Rapid action: Fast‑acting anesthetic effect suitable for topical, injectable and procedural applications.
Versatile applications: Used in both anesthesia and cardiac arrhythmia treatment.
Typical Applications:
Local Anesthetic Formulations: Injectable solutions, dental anesthesia, topical gels and creams for pain relief.
Antiarrhythmic Products: Component in intravenous formulations for emergency cardiac care.
Medical & Dental Products: Used in surgical, dermatological and dental procedures to reduce pain.
Pharmaceutical Manufacturing: Intermediate for advanced formulations and compounded drugs.
Physical & Chemical Properties:
Appearance: White to off‑white crystalline powder.
Solubility: Soluble in water and alcohol.
Melting Point: approx. 74‑82 °C.
pH (1 % aq. solution): ~4.0 – 5.5.
Packaging & Storage:
Available in 25 kg HDPE/fiber drums with protective liners or customized pharma packaging. Store in a cool, dry place away from moisture and direct sunlight.
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Mono Chloro Acetic Acid
Product Brochure
| Form | Powder |
| Purity | 99% |
| Chemical Formula | C2H3ClO2 |
| CAS NO | 79-11-8 |
| Molecular Weight | 94.49 g.mol-1 |
Mono Chloro Acetic Acid
Product Name: Mono Chloro Acetic Acid (MCA / MCAA)
CAS No: 79-11-8
Molecular Formula: C₂H₃ClO₂
Molecular Weight: 94.50 g/mol.
Product Overview:
Mono Chloro Acetic Acid (also known as Chloroacetic Acid or MCA/MCAA) is a high-purity, reactive organochlorine compound widely used in chemical manufacturing. It appears as a white to off-white crystalline solid with a characteristic pungent odor, and is highly soluble in water and common organic solvents.
Key Specifications:
Appearance: White crystalline powder or flakes.
Purity: Typically ≥ 99.0%.
Solubility: Freely soluble in water, alcohols, and ethers.
Melting Point: ~60–63 °C.
Boiling Point: ~189 °C.
CAS Number: 79-11-8.
Product Features:
Excellent quality with high assay value.
Compatible with industrial chemical processes.
Manufactured under strict quality control standards.
Supplied in stable crystalline/flake form for ease of handling.
Applications:
Mono Chloro Acetic Acid serves as a critical intermediate in numerous industrial and chemical processes:
Agrochemical Industry: used in the synthesis of herbicides, insecticides, growth regulators.
Chemical Industry: key raw material for carboxymethyl cellulose (CMC), surfactants, dyes, and intermediates.
Pharmaceuticals: used for manufacture of intermediates for drugs and fine chemicals.
Textiles & Paper: utilized in finishing agents and specialty chemical production.
Handling & Safety:
MCA is a corrosive and toxic acid. It must be handled with appropriate PPE (gloves, goggles, ventilation) and stored in airtight containers away from incompatible materials. Follow all relevant safety and regulatory guidelines.
Additional Information:
- Pay Mode Terms: L/C (Letter of Credit)
- Port of Dispatch: Ahmedabad
- Delivery Time: As per the order
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Clopidogrel Bisulphate Api
Product Brochure
| Grade Standard | IP |
| Purity | 99% |
| Molecular Weight | 419.891 g/mol |
| Formula | C16H16ClNO2S |
| PubChem CID | 115366 |
Product Name: Clopidogrel Bisulphate APISynonyms: Clopidogrel Hydrogen Sulfate, Clopidogrel Bisulfate, Clopidogrel Hydrogen Sulphate, Clopidogrel Sulfate, (S)-(+)-Methyl 2-(2-chlorophenyl)-2-(6,7-dihydro-4H-thieno[3,2-c]pyridin-5-yl)acetate Sulfate (1:1)CAS No.: 120202-66-6 Molecular Formula: C₁₆H₁₆ClNO₂S·H₂SO₄ Molecular Weight: ~419.9 g/mol Appearance: White to off-white crystalline powder Grade: Pharmaceutical / API Grade (USP/BP/EP compliant).
Product Description:
Clopidogrel Bisulphate API is a high-purity active pharmaceutical ingredient supplied as a white to off-white crystalline powder, manufactured to meet stringent global pharmacopoeial standards (USP, BP and EP). It is the bisulfate salt form of clopidogrel, a widely used antiplatelet agent that helps prevent harmful blood clots by blocking platelet activation and aggregation. Clopidogrel Bisulphate acts as a prodrug — once metabolized in the body, it selectively inhibits the binding of adenosine diphosphate (ADP) to P2Y₁₂ receptors on platelet surfaces, thereby reducing the risk of myocardial infarction, stroke and other thrombotic cardiovascular events.
Key Features:API-Grade Powder: High purity raw material for pharmaceutical formulations. White to Off-White Crystalline Powder: Easy to handle and process. Anti-Platelet Activity: Potent thienopyridine class agent that inhibits platelet aggregation. Pharmacopoeial Compliance: Meets quality specifications suitable for regulated markets. Stable Bulk Material: Consistent physical form and performance for large-scale API supply.
Typical Pharmaceutical Applications:Antithrombotic API: Used to manufacture oral solid dosage forms (tablets, capsules) that prevent clot formation. Cardiovascular Products: Core raw material in medicines for the treatment and prevention of atherosclerotic events. Combination Therapies: Often formulated with aspirin or other agents in cardiovascular care products. Pharmaceutical Manufacturing: Critical input for formulation lines requiring high-quality API.
Typical Physical & Chemical Properties:Appearance: White to off-white crystalline powder. Solubility: Freely soluble in methanol and acidic solutions; slight solubility in water. Assay: Typically ~97.0 – 101.5 % (dry basis) by HPLC (USP standard). Melting Point: ~174 – 184 °C. Optical Rotation: ~+52° to +56°.
Packaging & Storage:Available in export worthy packaging such as 25 kg/50 kg HDPE drums with liners or customized bulk packaging per buyer requirements. Store in a cool, dry place away from light and moisture to preserve quality and shelf life.
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Bronopol Usp Powder
Product Brochure
| Form | Powder |
| Grade Standard | Technical Grade |
| Physical State | Powder |
| Packaging Size | 25 kg |
| Packaging Type | Bag |
| Purity | 99% |
| Usage | Industrial |
| Molecular Formula | C3H6BrNO4 |
Product Name: Bronopol USP PowderSynonyms: 2‑Bromo‑2‑nitropropane‑1,3‑diol, Bronopol USP, BNPDCAS Number: 52‑51‑7 Molecular Formula: C₃H₆BrNO₄ Molecular Weight: ~199.99 g/mol Grade: USP / BP / IP compliant (pharmaceutical grade preservative) Physical Form: White to off‑white crystalline powder Assay (Purity): ≥99% (typically).
Product Description:
Bronopol is a high‑performance antimicrobial compound supplied as a white crystalline powder. It is widely used as an effective broad‑spectrum preservative and bactericide, with strong activity against bacteria, fungi, and algae. Its chemical name is 2‑bromo‑2‑nitropropane‑1,3‑diol and it is stable under recommended conditions for use in many formulations.
Key Features:High‑Purity USP Powder: Meets USP/BP/IP standards for pharmaceutical and preservative applications. Broad‑Spectrum Antimicrobial: Effective in controlling microbial contamination in formulations. White Crystalline Powder: Easy to handle and incorporate into solid or liquid formulations. Stable & Water Soluble: Soluble in water and compatible with polar solvent systems.
Applications:Pharmaceutical Preservative: Used in topical pharmaceutical products to prevent microbial growth and increase shelf life. Cosmetics & Personal Care: Employed as a preservative in creams, shampoos, lotions, and other personal care formulations at low concentrations. Industrial Uses: Functions as a microbiocide in water treatment, cooling towers, oil and gas systems, paper mills, and other industrial applications. Surface Sanitizers & Cleaners: Added to disinfectant and surface sanitization products to enhance antimicrobial efficacy.
Typical Specification (Indicative):Assay (HPLC): ≥ 99.0% Appearance: White to off‑white crystalline powder Melting Point: ~130–133 °C Solubility: Soluble in water; sparingly soluble in alcohols and other polar solvents.
Storage & Handling:Store in a cool, dry, and well‑ventilated area away from heat, moisture and direct sunlight. Keep containers tightly closed to maintain product quality. Handle with appropriate personal protective equipment (PPE) such as gloves and eye protection.
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Tamoxifen Citrate Api
Product Brochure
| Grade Standard | Technical Grade |
| Packaging Type | Barrel |
| Usage/Application | Laboratory |
| Purity | 99% |
| Physical State | Powder |
| Assay | 100% |
| Packaging Size | 250 Ltr |
| Molar Mass | 371.515 g/mol |
| Formula | C26H29NO |
Product Name: Tamoxifen Citrate API.CAS No.: 54965-24-1.
Product Description:
Tamoxifen Citrate is an active pharmaceutical ingredient (API) belonging to the class of selective estrogen receptor modulators (SERMs) with potent antiproliferative and antitumor properties. It is widely used in the manufacture of anti-breast cancer formulations, and is a key raw material for therapeutic applications in oncology.
Chemical & Physical Properties:Chemical Name: (Z)-2-[4-(1,2-Diphenyl-1-butenyl)phenoxy]-N,N-dimethylethanamine citrate. Molecular Formula: C26H29NO·C6H8O7. Molecular Weight: ~563.64 g/mol. Appearance: White to off-white crystalline powder. Solubility: Soluble in methanol; slightly soluble in ethanol; very slightly soluble in water. Melting Point: ~140–148 °C.
Key Features:High-purity API for pharmaceutical manufacturing & research use. Manufactured under cGMP/ISO quality standards (depending on supplier). Suitable for oncology drug formulations and intermediates.
Pharmacological Role:Tamoxifen citrate is a selective estrogen receptor modulator (SERM) that:Blocks estrogen receptors on breast cancer cells.Prevents estrogen-stimulated tumor growth.Is extensively used in hormone-dependent breast cancer treatment and adjuvant therapy.
Usage & Handling:For manufacturing and laboratory use only (not for direct consumption).Store in a cool, dry place at controlled temperature (e.g., 2–8 °C). Follow all regulatory, safety and compliance standards for APIs during handling.
Packaging & Supply:Typically supplied in:Drum, Bag, or HDPE containers.Custom packaging available upon request.Bulk quantities supported for commercial orders.
Applications:Oncology drug formulations.Pharmaceutical intermediate for breast cancer medicines.Research & development API supply.
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Chlorzoxazone Powder IP/BP/USP/EP
Product Brochure
| Purity | 99% |
| Assay | 40% |
| Molar Mass | 169.565 g/mol |
| Country of Origin | Made in India |
| Formula | C7H4ClNO2 |
| Grade Standard | USP |
Product Name: Chlorzoxazone Powder APICAS No.: 95-25-0.Synonyms: 5-Chloro-2-benzoxazolone; Paraflex; Mioran.Grade: IP / BP / USP (Pharmaceutical-Grade).
Product Overview:
Chlorzoxazone Powder API is a high-quality active pharmaceutical ingredient (API) used in the manufacture of muscle relaxant medicines. It is a centrally acting skeletal muscle relaxant that helps relieve pain and stiffness caused by muscle strains and spasms.
Chemical & Physical Properties:Chemical Name: Chlorzoxazone.Molecular Formula: C₇H₄ClNO₂.Molecular Weight: ~169.56–169.57 g/mol. Appearance: White to off-white crystalline powder. Purity: Typically ≥98% (or as specified) depending on supplier. Melting Point: ~191–192 °C. Solubility: Slightly soluble in water; soluble in common organic solvents such as ethanol, acetone, chloroform.
Key Features & Benefits:Pharmaceutical-grade API: Suitable for formulation into solid oral dosage forms such as tablets and capsules. Consistent quality & purity: Manufactured to meet pharmacopeial standards (IP/BP/USP) with documentation like COA/MSDS available on request. Stable powder form: Micronized and easy for handling and processing. Long shelf life: Stable under recommended storage conditions (cool, dry, away from light).
Usage & Handling:Intended strictly for pharmaceutical manufacturing and R&D use (not for direct ingestion in raw form).Store in a cool, dry, well-ventilated place, protected from moisture and direct sunlight.Follow applicable safety and regulatory standards during handling.
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Chlorpheniramine Maleate Api
Product Brochure
| Grade Standard | USP |
| Purity | Greater than 99% |
| Packaging Type | Drum |
| Country of Origin | Made in India |
| Colour | white |
Product Name: Chlorpheniramine MaleateCAS Number: 113-92-8 Synonyms: Chlorphenamine Maleate, Chlorpheniramine, Chlorprophenpyridamine Molecular Formula: C₁₆H₁₉ClN₂ · C₄H₄O₄ Molecular Weight: ~390.86 g/mol Appearance: White to off-white crystalline powder Grade: Pharmaceutical API – IP / BP / USP available Purity: Typically ≥ 98–99 % (assay on dried basis)
Description:
Chlorpheniramine Maleate is a first-generation antihistamine API widely used in the pharmaceutical industry for the manufacture of allergy relief medications and related therapeutic products. It acts by blocking H₁ histamine receptors, helping to reduce symptoms caused by excessive histamine release during allergic responses, such as sneezing, itching, runny nose, and watery eyes.
Key Features & Benefits:Therapeutic Category: Antihistaminic API Form: White or almost white crystalline powder Solubility: Freely soluble in water and alcohol Melting Point: ~130 – 135 °C Assay / Purity: Meets high pharmaceutical standards (e.g., ≥ 98 %) Stability: Stable when stored under recommended conditions in original packaging COA / MSDS: Available upon requestApplications:Chlorpheniramine Maleate API is extensively used in the formulation of:Allergy relief tablets, capsules, syrups and suspensions.Cold and flu medicines.Respiratory care combinations (where permitted).Veterinary antihistamine products.
Storage & Handling:Store in a cool, dry place away from direct sunlight and moisture. Packaged in protective liners and drums to maintain integrity during transport and storage.
Typical Packaging:25 kg / 50 kg HDPE drums with double liners.Fiberboard drums.Corrugated boxes (custom packaging on request).
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