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Lidocaine Base IP – Active Pharmaceutical Ingredient
Product Name: Lidocaine Base (IP Grade)CAS Number: 137-58-6 Molecular Formula: C₁₄H₂₂N₂O Molecular Weight: 234.34 g/mol Pharmacopoeia Standard: IP (Indian Pharmacopoeia) / BP / USP / EP Grade: IP Pharmaceutical Grade API Appearance: White to off-white crystalline powder. Purity: ≥99% (Typical assay) Packaging: 25 kg HDPE drum / Fiber drum (export standard).

Description:
Lidocaine Base IP is a high-quality Active Pharmaceutical Ingredient (API) used in the formulation of local anesthetics and antiarrhythmic drugs. It is produced to meet the Indian Pharmacopoeia (IP) standards, ensuring compliance with regulatory requirements for pharmaceutical manufacturing in India and for export. Chemically, Lidocaine is an amide-type local anesthetic that works by blocking voltage-gated sodium channels in nerve fibers, thereby inhibiting the initiation and conduction of nerve impulses which results in effective local numbness and anesthesia.
Key Features & Benefits:IP Compliant API — Manufactured in accordance with Indian Pharmacopoeia standards for pharmaceutical use. High Purity & Consistency — Typically ≥99% assay ensures dependable performance in finished formulations. Versatile Application — Used in topical, injectable, and other dosage forms for pain relief and anesthesia. Broad Pharmaceutical Use — Suitable for creams, gels, ointments, sprays, patches, and injectables. Stable & Reliable — Good shelf-life and stability under recommended storage conditions. 
Applications:Local anesthesia in minor surgical procedures, dental applications, and dermatological treatments. Formulation of topical analgesics (creams, ointments, gels) to relieve itching, pain or burning. Intermediate for pharmaceutical synthesis and compounding.
Storage & Handling:Store in a cool, dry, well-ventilated place away from direct heat and moisture. Ensure packaging is sealed when not in use to maintain quality and stability.

Lidocaine Base API — Active Pharmaceutical Ingredient
Product Name: Lidocaine Base APICAS Number: 137-58-6 Molecular Formula: C₁₄H₂₂N₂O Molecular Weight: ~234.34 g/mol IUPAC Name: 2-(diethylamino)-N-(2,6-dimethylphenyl) acetamide Synonyms: Lidocaine, Lignocaine, Xylocaine Appearance: White to off-white crystalline powder. Grade: Pharma / IP / BP / USP / EP (as per customer requirement). Purity: ≥99% (Pharmaceutical grade). Packaging: 25 kg HDPE drum (export. standard) / custom packaging available.

Description:
Lidocaine Base is a widely used local anesthetic API of the amide type, employed in the manufacturing of pharmaceutical formulations for pain management and minor surgical procedures. It acts by blocking voltage-gated sodium channels in nerve cells, interrupting pain signal transmission and providing effective local or regional anesthesia. This API is essential in the production of injectable solutions, topical gels, creams, ointments, sprays, and patches designed to provide rapid onset pain relief.
Key Features & Benefits:High-Purity API — Meets stringent pharmacopoeial standards (IP/BP/USP/EP). Effective Local Anesthetic — Provides rapid and reliable pain control. Versatile Applications — Used in dermatological, dental, surgical, and emergency care formulations. Fast Onset of Action — Quickly numbs targeted areas for efficient procedural use. Stable & Well-Characterized — Good shelf life with consistent performance in finished formulations. Cost-Effective — Ideal for bulk API requirements in pharmaceutical manufacturing.
Typical Applications:Local and regional anesthesia in minor medical and dental procedures. Topical analgesic products (creams, gels, sprays). Used as API in formulations to manage certain cardiac arrhythmias (class-IB antiarrhythmic). Intermediate in pharmaceutical synthesis and compound development. 
Storage & Handling:Store in a cool, dry place away from direct sunlight. Ensure containers are tightly sealed to maintain stability and potency. Handle with appropriate safety measures according to good manufacturing practices.

Benzocaine API Powder – Pharmaceutical Grade
Product Name: Benzocaine API Powder.Chemical Name: Ethyl 4-aminobenzoate.CAS Number: 94-09-7Molecular Formula: C₉H₁₁NO₂Appearance: White to off-white crystalline powder.Grade: Pharmaceutical / USP/BP standard.Purity: ≥ 99.0% (or as per customer requirement)

Description:

Benzocaine API Powder is a high-quality active pharmaceutical ingredient widely used in the formulation of topical local anesthetic products. It provides rapid and effective temporary pain relief by blocking peripheral nerve signals, making it ideal for use in dental gels, throat lozenges, sprays, ointments, and other pain relief formulations.
Key Features:High purity meeting pharmacopeial standards (USP/BP).Fine, consistent particle size for easy formulation.Stable, free-flowing powder suitable for bulk processing.Excellent compatibility with excipients and  solvents.
Reliable quality with Certificate of Analysis (COA).
Applications:Topical analgesic and anesthetic formulations.Dental and oral care gels, lozenges, and sprays.OTC pain relief products.Pharmaceutical manufacturing and contract formulation.
Packaging & Storage:Available in 1 kg, 5 kg, 25 kg drum or customized packing.Store in a cool, dry place, away from direct sunlight.Shelf life: Standard 2–3 years under recommended conditions.

Guaifenesin API Powder
Product Name: Guaifenesin USP 36 Powder Bulk (Guaifenesin API Powder)CAS No.: 93-14-1.Synonyms: Guaiphenesin, Glyceryl guaiacolate, 3-(2-Methoxyphenoxy)-1,2-propanediol.Grade: IP / BP / USP / Pharma-Grade Active Pharmaceutical Ingredient.

Product Overview:
Guaifenesin API Powder is a high-quality active pharmaceutical ingredient widely used in the pharmaceutical industry for the formulation of expectorant medicines. It is a key raw material in the manufacture of cough and cold therapeutic products and is valued for its ability to help loosen and thin mucus in the airways, making it easier to cough up and clear congestion.
Chemical & Physical Properties:Chemical Name: 3-(2-Methoxyphenoxy)-1,2-propanediol. Molecular Formula: C₁₀H₁₄O₄. Molecular Weight: ≈ 198.22 g/mol. Appearance: White to slightly gray crystalline powder. Melting Point: ~78–82 °C. Solubility: Soluble in water, alcohol and some organic solvents. Assay: Typically ≥ 98–99 %. 
Key Features & Benefits:Pharmaceutical-grade API compliant with global pharmacopeial standards (IP/BP/USP). High chemical purity and consistent quality for reliable formulation results. Supplied in stable crystalline powder form for easy handling and processing. Suitable for incorporation into a wide range of finished dosage forms such as tablets, capsules, syrups, and powders. Long shelf life when stored under recommended conditions (cool, dry, and away from light).
Usage & Handling:For pharmaceutical manufacturing and R&D use only.Store in a clean, cool, dry area in tightly closed containers. Use appropriate personal protective equipment (PPE) during handling.Follow standard regulatory and safety protocols.

Ropivacaine HCl Monohydrate – Product Description
Product Name: Ropivacaine Hydrochloride MonohydrateGrade: Pharma API / EP / BP / USP (depending on requirement)Synonyms: Ropivacaine HCl·H₂O, (S)-Ropivacaine Hydrochloride. Monohydrate, LEA-103 · Naropin HCl Monohydrate.CAS Number: 132112-35-7. Molecular Formula: C₁₇H₂₆N₂O · HCl · H₂O. Molecular Weight: ~328.88 g/mol. Appearance: White to off-white crystalline powder.

Description:
Ropivacaine HCl Monohydrate is a high-quality active pharmaceutical ingredient (API) belonging to the amide class of local anesthetics, widely used in the formulation of injectable anesthetic solutions. As the pure S-(-)-enantiomer, it offers long-acting local anesthesia with a favorable sensory versus motor blockade profile and relatively reduced cardiotoxicity compared to some traditional anesthetics.
Key Features & Benefits:High Purity API: Typically ≥98% pharmaceutical grade (USP/EP/BP standards available). Potent Local Anesthetic: Acts by reversibly blocking sodium ion influx in nerve fibers, inhibiting nerve impulse conduction.Enhanced Safety Profile: Compared with certain other local anesthetics, it offers a greater motor-sensory differentiation† and lowered systemic toxicity.Wide Use in Anesthetic Formulations: Preferred in epidural, spinal, and peripheral nerve block applications.Stable Form: Crystalline monohydrate form with good handling and formulation characteristics.
Typical Specifications (Indicative):Assay (Purity): Conforms to pharmacopoeial limits (e.g., 98.5–101%) Appearance: White to off-white crystalline powder. Solubility: Soluble in water and ethanol; formulation dependent.Optical Purity: Conforms to defined enantiomeric standards (especially in EP/USP monographs).
Packaging & Storage:Standard Packaging: 10 kg / 25 kg / 50 kg HDPE drums with inner liners or per customer requirement.Storage Conditions: Store in a cool, dry, well-sealed container, protected from moisture and light.Shelf Life: As per manufacturer specification (typically 2 + years under proper conditions).

Prilocaine API – BP Grade (Active Pharmaceutical Ingredient)
Product Name: Prilocaine APISynonyms: Prilocaine, α-n-Propylamino-2-methylpropionanilide, Prilocain, PropitocaineCAS Number: 721-50-6 Molecular Formula: C₁₃H₂₀N₂O Molecular Weight: 220.31 g/mol Grade: BP (British Pharmacopoeia) compliant API (also available in IP/USP/EP grade) Physical Form: White to off-white crystalline powder. Purity: ≥99% typical pharmaceutical grade.

Description:
Prilocaine BP is a pharmaceutical active ingredient belonging to the amide class of local anesthetics used extensively in the manufacture of local anesthetic formulations. It is designed to provide temporary and localized loss of sensation by blocking voltage-gated sodium channels in nerve membranes, thereby inhibiting nerve impulse conduction. Prilocaine is widely used in dental anesthesia, minor surgical procedures, and topical applications. It is also frequently combined with other anesthetics like lidocaine to enhance efficacy in dermal anesthesia products.
Key Features:BP Grade API: Complies with British Pharmacopoeia quality standards; also available in IP/USP/EP pharmacopeial grades based on customer requirements. High Purity & Consistent Quality: Manufactured under controlled conditions for reliable pharmaceutical performance. Therapeutic Category: Local anesthetic API used for formulation of injectable, topical creams, gels, and combination anesthetic products. Physical Form: White crystalline powder suitable for efficient handling and formulation processes. 
Applications:Pharmaceutical Manufacturing: Used as the core active ingredient in local anesthetic drugs for dental, surgical, and procedural pain management. Combination Formulations: Often formulated with other anesthetics (e.g., lidocaine) for enhanced topical anesthesia. Research & Development: Employed in formulation development, quality control, and analytical studies for finished pharmaceutical products.Generic & Branded Products: Suitable for both generic production and branded anesthetic drug manufacturing.
Storage & Handling:Store in a cool, dry place away from moisture and direct sunlight. Ensure the product is kept in sealed, original packaging to preserve quality and prevent contamination.

Riboflavin Sodium Phosphate API Powder – IP/BP/USP Grade
Product Name: Riboflavin Sodium Phosphate (Riboflavin 5′-Phosphate Sodium)Synonyms: Riboflavin monophosphate monosodium salt, Vitamin B2 Sodium Phosphate, Vitamin B₂ 5′-Phosphate SodiumCAS Number: 130-40-5 Molecular Formula: C₁₇H₂₀N₄NaO₉P Molecular Weight: ≈ 478.33 g/mol Appearance: Yellow to orange-yellow crystalline hygroscopic powder Grade: IP / BP / USP / EP (Available on request) Assay: Typically 73–80% on dry basis (per pharmacopeial specifications) Solubility: Soluble in water; very slightly soluble in ethanol; practically insoluble in ether Packaging: 1 kg – 25 kg bags or fiber drums (custom packaging available)

Product Description:
Riboflavin Sodium Phosphate API Powder is a high-quality active pharmaceutical and nutritional ingredient manufactured in compliance with IP (Indian Pharmacopoeia), BP (British Pharmacopoeia), and USP (United States Pharmacopeia) standards. It appears as a yellow to orange-yellow crystalline powder with excellent water solubility and stability — making it versatile for pharmaceutical, nutraceutical, and food fortification applications. This compound is the sodium phosphate salt of riboflavin (Vitamin B2), a water-soluble vitamin essential for cellular metabolism and energy production. The phosphate form enhances solubility and bioavailability compared to free riboflavin, and is widely used in formulations requiring water-soluble vitamin APIs.
Key Features & Benefits:Pharmacopeial Compliance: Meets IP, BP, and USP quality standards for active pharmaceutical ingredients. Water-Soluble Powder: Excellent solubility enables easy formulation in liquid, oral, and parenteral dosage forms. Enhanced Bioavailability: Phosphate form of Vitamin B2 supports efficient absorption and metabolic activity. Stable & Reliable: Controlled quality with consistent assay ensures dependable performance in finished products. Versatile Usage: Applicable across pharmaceutical, nutraceutical, and fortified food product lines. Custom Packaging: Flexible packaging options available to suit export and domestic requirements.
Applications:Pharmaceutical API — Used in multivitamin formulations, vitamin supplements, and therapeutic products. Nutraceuticals & Fortified Foods — Added to beverages, dairy products, cereals, and infant nutrition products for vitamin enrichment. Cosmetics & Personal Care — Incorporated in topical products for skin health and antioxidant support. Veterinary & Animal Nutrition — Included in feed premixes for poultry and livestock growth support. 
Storage & Handling:Store in a cool, dry, and well-ventilated area, away from direct sunlight, moisture, and heat. Keep containers tightly closed when not in use to preserve product integrity and extend shelf life.

Lidocaine Base BP – Active Pharmaceutical Ingredient (API)
Product Name: Lidocaine Base BPOther Names: Lignocaine Base, Xylocaine BaseCAS Number: 137-58-6 Molecular Formula: C₁₄H₂₂N₂O Molecular Weight: 234.34 g/mol Pharmacopoeial Standard: British Pharmacopoeia (BP) – Pharmaceutical GradeAppearance: White to off-white crystalline powder Purity (Assay): ≥99% (Typical)Grade: BP / USP / EP / IP (as per customer requirement)Packaging: 25 kg HDPE drum / Fiber drum – export quality.

Description:
Lidocaine Base BP is a high-quality active pharmaceutical ingredient (API) manufactured to meet stringent British Pharmacopoeia (BP) standards for pharmaceutical use. It is an amide-type local anesthetic widely used as a raw material in the production of anesthetic formulations. Lidocaine works by blocking voltage-gated sodium channels on nerve cells, inhibiting nerve impulse transmission to provide effective local or regional anesthesia. This BP grade API is suitable for pharmaceutical manufacturing where compliance with British Pharmacopoeia specifications is required for regulatory approval and quality assurance. High-purity and consistent quality make it ideal for use in both domestic and export markets.
Key Features & Benefits:BP-Certified API — Conforms to British Pharmacopoeia standards for identity, purity, and quality.High Purity & Consistency — Ensures reproducible performance in finished formulations.Versatile Use — Suitable for topical, injectable, and other dosage form formulations.Reliable Raw Material — Ideal for manufacturing local anesthetic products such as creams, gels, ointments, sprays, and injectables.Pharma-Grade Quality — Meets international pharmacopeial standards (BP, USP, EP, IP).Export-Ready Packaging — Secure packaging to maintain product integrity during transit.
Applications:Local anesthetics for medical, dental, and surgical procedures.API in topical analgesic formulations (creams, gels, sprays).Intermediate in pharmaceutical synthesis and industrial production.Used in products requiring BP-compliant raw materials for regulatory approval.
Storage & Handling:Store in a cool, dry, well-ventilated area away from heat, moisture, and direct sunlight. Keep containers tightly closed when not in use to preserve product stability and prevent contamination.

Bupivacaine HCl Monohydrate API USP – Product Description
Product Name: Bupivacaine Hydrochloride Monohydrate APIGrade: USP (United States Pharmacopeia) / Pharma GradeCAS Number: 73360-54-0. Molecular Formula: C₁₈H₂₈N₂O·HCl·H₂O. Molecular Weight: 342.9 g/mol. Appearance: White to off-white crystalline powder. Purity: Typically ≥ 98 % (Pharma Grade).

Description:

Bupivacaine Hydrochloride Monohydrate API USP is a high-quality active pharmaceutical ingredient (API) used in the development and manufacture of local anesthetic formulations. It belongs to the amide class of local anesthetics and is widely employed in medical and pharmaceutical applications to provide long-acting anesthesia and pain relief during surgical procedures and postoperative care. Bupivacaine HCl Monohydrate API USP is supplied as a white, odorless crystalline powder with excellent solubility properties in water and ethanol, suitable for formulating injectable products after appropriate compounding.
Key Features & Benefits:Pharmacopeial Compliance: Conforms to USP quality and purity standardsConsistent Quality: High purity and reproducible performance in formulations. Long-Acting Anesthetic: Provides extended duration of local anesthesia compared to many other anesthetics. Suitable for Injectable Formulations: Ideal API for epidural, spinal and peripheral nerve block anesthesia applications. Stable Powder Form: Easy handling, storage, and formulation processing.
Technical Specifications:Appearance: White to off-white crystalline powder. Assay (Purity): ≥ 98 % (typical USP pharma grade). Solubility: Soluble in water and ethanol; slightly soluble in chloroform or acetone pH (1% Solution): Typically within USP specified limits.Moisture Content: Controlled per USP guidelines.
Packaging & Storage:Standard Packaging: 1 kg / 5 kg / 25 kg HDPE drums with inner liners (custom packaging on request).Storage Conditions: Store in a cool, dry, well-sealed container away from moisture, light, and heat.Shelf Life: Typically 2+ years under recommended storage.