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Guaifenesin IP USP WHO GMP
Guaifenesin IP USP WHO GMP

Guaifenesin IP USP WHO GMP

Price 1000 INR/ Kilograms

MOQ : 100 Kilograms

Guaifenesin IP USP WHO GMP Specification

  • HS Code
  • 29329910
  • Melting Point
  • 78-82C
  • EINECS No
  • 202-222-5
  • Ingredients
  • Guaifenesin
  • Ph Level
  • 5.0 - 7.0 (1% solution)
  • Grade
  • IP/USP/WHO-GMP
  • Shelf Life
  • 36 months
  • Storage
  • Store in a cool, dry, and well-ventilated area, away from sunlight
  • Shape
  • Crystalline
  • Properties
  • Expectorant, increases volume and reduces viscosity of secretions in trachea and bronchi
  • Density
  • 1.293 Gram per cubic centimeter(g/cm3)
  • Product Type
  • Active Pharmaceutical Ingredient (API)
  • Poisonous
  • NO
  • CAS No
  • 93-14-1
  • Appearance
  • White crystalline powder
  • Usage
  • Used in cough syrups, tablets, and other oral dosage forms
  • Physical Form
  • Powder
  • Taste
  • Slightly bitter
  • Solubility
  • Freely soluble in water, sparingly soluble in alcohol
  • Molecular Formula
  • C10H14O4
  • Smell
  • Odorless
  • Application
  • Pharmaceutical formulations, especially as an expectorant
  • Molecular Weight
  • 198.22 g/mol
  • Structural Formula
  • HOCH2C6H4OCH2OCH3
  • Purity
  • >=99%
  • Packing Details
  • 25kg fiber drum with double inner polythene bags
  • Standard Certification
  • WHO-GMP certified manufacturing
  • Loss On Drying
  • Not more than 0.5%
  • Microbial Limits
  • Complies with pharmacopeial standards
  • Residual Solvents
  • Complies with ICH Q3C guidelines
  • Identification Methods
  • IR, HPLC, UV
  • Heavy Metals
  • Not more than 10 ppm
 

Guaifenesin IP USP WHO GMP Trade Information

  • Minimum Order Quantity
  • 100 Kilograms
  • FOB Port
  • mudara
  • Payment Terms
  • Cash in Advance (CID), Letter of Credit at Sight (Sight L/C), Letter of Credit (L/C)
  • Supply Ability
  • 1000 Kilograms Per Month
  • Delivery Time
  • 7 Days
  • Main Export Market(s)
  • Asia, Australia, South America, Eastern Europe, Africa
  • Main Domestic Market
  • North India, East India, Gujarat, Karnataka, Kerala, Lakshadweep, Mizoram, Meghalaya, Manipur, Andhra Pradesh, Bihar, Chandigarh, Daman and Diu, Goa, Jharkhand, Odisha, Punjab, Assam, Delhi, Dadra and Nagar Haveli, Andaman and Nicobar Islands, Arunachal Pradesh, Chhattisgarh, Haryana, Himachal Pradesh, Jammu and Kashmir, Madhya Pradesh, Maharashtra, Nagaland, Rajasthan, All India, South India, Central India, West India
 

Guaifenesin IP USP WHO GMP About



Guaifenesin IP USP WHO GMP is a must-have for pharmaceutical manufacturers seeking extraordinary quality. Boasting a radiant white crystalline appearance, this IP/USP/WHO-GMP grade compound is renowned for its soaring purity level of 99% or above. Capitalise on the benefits of a product that complies with WHO-GMP standards, offering safety and efficacy through strict microbial, heavy metal, and solvent controls. Get It Now in a 25kg fiber drum with double inner polythene bags-ideal for cough syrups and oral formulations. Experience reliable, odourless, and efficient expectorant action, certified for global export.

Advanced Applications & Competitive Edge of Guaifenesin IP USP WHO GMP

Guaifenesin IP USP WHO GMP stands out for use in pharmaceutical plants, especially due to its role as an expectorant in cough syrups and tablets. It offers producers a competitive advantage by ensuring extraordinary purity and consistent efficacy in application media such as liquid and solid oral dosage forms. Its compliance with stringent pharmacopeial standards elevates manufacturing reliability and product valuation worldwide.


Packaging, Export Valuation & Steady Supply of Guaifenesin IP USP WHO GMP

Supplied in secure 25kg fiber drums lined with double inner polythene bags, Guaifenesin IP USP WHO GMP reaches valuation benchmarks ideal for export worldwide. Benefit from prompt quotations tailored to market needs in Europe, Asia, the Middle East, and Africa. A robust supply chain ensures consistent availability, facilitating smooth distribution cycles and efficient stock maintenance for international partners.


FAQ's of Guaifenesin IP USP WHO GMP:


Q: How is Guaifenesin IP USP WHO GMP typically used in pharmaceutical formulations?

A: Guaifenesin IP USP WHO GMP is primarily used as an expectorant in cough syrups, tablets, and other oral dosage forms, functioning to increase the volume and reduce the viscosity of bronchial secretions.

Q: What sets the quality of this Guaifenesin apart from others in the market?

A: This Guaifenesin meets rigorous WHO-GMP, IP, and USP standards for purity (99%), safety, and compliance with strict limits on heavy metals, microbial contamination, and residual solvents.

Q: Where do you export Guaifenesin IP USP WHO GMP?

A: We export Guaifenesin IP USP WHO GMP globally, with major markets in Europe, Asia, the Middle East, and Africa, catering to pharmaceutical manufacturers and distributors.

Q: What are the recommended storage conditions for this product?

A: Guaifenesin IP USP WHO GMP should be stored in a cool, dry, and well-ventilated area away from sunlight to maintain its shelf life and integrity.

Q: How can customers request a quotation or supply details for Guaifenesin?

A: Customers can obtain a product valuation or customized quotation by reaching out to our sales team with their requirements, and supply logistics are planned for seamless delivery worldwide.

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