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ONDANSETRON HCL BASE IP
ONDANSETRON HCL BASE IP

ONDANSETRON HCL BASE IP

Price 1800 INR/ Kilograms

MOQ : 25 Kilograms

ONDANSETRON HCL BASE IP Specification

  • Molecular Weight
  • 365.86 g/mol
  • Molecular Formula
  • C18H19N3O.HCl
  • Assay
  • >99%
  • Residue on Ignition
  • NMT 0.1%
  • HS Code
  • 29349900
  • Loss on Drying
  • NMT 0.5%
  • Moisture (%)
  • NMT 0.5%
  • Place of Origin
  • India
  • Heavy Metal (%)
  • NMT 0.001%
  • Melting Point
  • 178-180C
  • Storage
  • Store in cool, dry place
  • Other Names
  • Ondansetron Hydrochloride Base IP
  • CAS No
  • 99614-01-4
  • Type
  • Pharmaceutical Raw Material
  • Grade
  • IP (Indian Pharmacopoeia)
  • Usage
  • Anti-emetic, Active Pharmaceutical Ingredient
  • Purity
  • >99% (HPLC)
  • Appearance
  • White to Off-White Powder
  • Application
  • Pharmaceutical Formulations
  • Raw Material
  • Yes
  • Smell
  • Odorless
  • Color
  • White to Off-White
  • Form
  • Powder
  • Storage Condition
  • Protected from light and moisture
  • Solubility
  • Soluble in water and methanol
  • Sulfated Ash
  • NMT 0.1%
  • Microbial Limit
  • Complies with IP Specifications
  • Identification
  • Positive as per IP Specifications
  • Impurities
  • Complies with IP Limits
  • Shelf Life
  • 36 Months from date of Manufacture
  • Packaging
  • HDPE Drums with double polybags
 
 

About ONDANSETRON HCL BASE IP

Ondansetron Hydrochloride (HCl) Base, as defined by the Indian Pharmacopoeia (IP), is a pharmaceutical substance categorized as a serotonin 5-HT3 receptor antagonist. It is primarily used to prevent nausea and vomiting induced by chemotherapy, radiotherapy, and surgery. The IP provides comprehensive specifications to ensure the quality, potency, and safety of Ondansetron HCl Base for medicinal use.

Quality and Compliance

Ondansetron HCL Base IP complies with Indian Pharmacopoeia specifications, ensuring high purity and minimal impurities, heavy metals, and moisture. Each batch is carefully tested to meet or exceed regulatory standards for pharmaceutical raw materials, making it a reliable choice for pharmaceutical formulation.


Optimal Storage and Packaging

The product is protected from light and moisture by packaging in HDPE drums with double polybags. Proper storage conditions and robust packaging help maintain the stability and effectiveness of the Ondansetron HCL Base IP over its 36-month shelf life.


Versatile Pharmaceutical Applications

Ondansetron HCL Base IP serves as an active pharmaceutical ingredient in anti-emetic medications, making it essential for preventing and treating nausea and vomiting. Its high solubility in water and methanol allows seamless integration into various pharmaceutical formulations.

FAQ's of ONDANSETRON HCL BASE IP:


Q: How should Ondansetron HCL Base IP be stored to retain its quality?

A: Ondansetron HCL Base IP should be stored in a cool, dry place, protected from light and moisture. Its packaging in HDPE drums with double polybags ensures optimal preservation and extends its shelf life up to 36 months from the date of manufacture.

Q: What is the primary usage of Ondansetron HCL Base IP in pharmaceuticals?

A: Ondansetron HCL Base IP is widely used as an active ingredient in anti-emetic pharmaceutical formulations, particularly for preventing and treating nausea and vomiting associated with chemotherapy, surgery, or other medical conditions.

Q: When does the shelf life of Ondansetron HCL Base IP expire?

A: The shelf life of Ondansetron HCL Base IP is 36 months from the date of manufacture, provided that storage conditions are maintained properly as per the recommended guidelines.

Q: Where is Ondansetron HCL Base IP commonly manufactured and supplied?

A: Ondansetron HCL Base IP is manufactured, supplied, and traded predominantly in India, and conforms to the Indian Pharmacopoeia (IP) standards for pharmaceutical ingredients.

Q: What benefits does the high purity (>99%) of Ondansetron HCL Base IP offer?

A: High purity ensures the consistent effectiveness, safety, and quality of pharmaceutical products, minimizing the risk of impurities or contaminants in anti-emetic medications formulated with Ondansetron HCL Base IP.

Q: How is the quality and impurity profile of Ondansetron HCL Base IP maintained?

A: Quality is maintained through rigorous compliance with IP limits for impurities, heavy metals, sulfated ash, and microbial content. Each batch undergoes thorough analytical testing, ensuring alignment with regulatory specifications.

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