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Famotidine Api

Famotidine Api

Product Details:

  • Shelf Life 5 Years
  • Medicine Name Famotidine
  • CAS No 76824-35-6
  • Type Pharmaceutical Intermediates
  • Grade Medicine Grade
  • Usage Antiulcer
  • Purity(%) 99
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Famotidine Api Price And Quantity

  • 25 Kilograms

Famotidine Api Product Specifications

  • Pharmaceutical Intermediates
  • Medicine Grade
  • A White or yellowish white crystalline
  • 99
  • 76824-35-6
  • 5 Years
  • Famotidine
  • Antiulcer
  • Powder

Famotidine Api Trade Information

  • MUMBAI
  • Western Union, Paypal, Cash in Advance (CID), Cash Advance (CA)
  • 500 Kilograms Per Week
  • 15 Days
  • 25kg/drum with double plastic bags inside; packed in a cardboard drum or fiber HDPE drum.
  • Australia, North America, South America, Eastern Europe, Western Europe, Middle East, Africa, Central America, Asia
  • All India

Product Description

Famotidine is given to surgery patients before operations to prevent postoperative nausea and to reduce the risk of aspiration pneumonitis. Famotidine is also given to some patients taking NSAIDs to prevent peptic ulcers. It serves as an alternative to proton-pump inhibitors. It is also given to dogs and cats with acid reflux. Famotidine has also been used in combination with an H1 antagonist to treat and prevent urticaria caused by an acute allergic reaction.

Key Applications in Pharmaceuticals

Famotidine API is primarily used in the development of antiulcer medicines. Its high pharmaceutical grade ensures safety and effectiveness in medical formulations. This compound acts as an H2 receptor antagonist, which helps reduce the production of stomach acid, providing relief from conditions like ulcers, GERD, and other related gastrointestinal issues. Pharmaceutical companies value its reliable performance and stable shelf life.


Quality Assurance and Purity

Tested for a purity of 99%, this API meets stringent quality standards necessary for medicinal products. Its physical form as a crystalline powder ensures uniformity in formulation and ease of integration into various dosage forms. The medicine grade classification guarantees that the ingredient is suitable for sensitive medical applications and long-term storage, with a five-year shelf life.

FAQ's of Famotidine Api:


Q: How is Famotidine API typically used in the pharmaceutical industry?

A: Famotidine API is mainly employed as an intermediate in the production of antiulcer drugs. It is incorporated into formulations to help reduce stomach acid, targeting conditions such as ulcers and gastroesophageal reflux disease (GERD).

Q: What benefits does Famotidine API offer for medication manufacturers?

A: With a high purity level of 99% and a stable shelf life of five years, Famotidine API ensures consistent drug efficacy, safety, and formulation stability, which are essential for producing reliable antiulcer medications.

Q: When should Famotidine-based medications be considered for use?

A: Famotidine-containing medicines are prescribed when patients need treatment for excessive stomach acid production, ulcers, heartburn, or GERD-related symptoms, as advised by healthcare professionals.

Q: Where can I source high-quality Famotidine API?

A: This pharmaceutical intermediate is available through established exporters, suppliers, and traders in India, who comply with industry and regulatory standards for quality assurance.

Q: What is the typical appearance and form of Famotidine API used in medicines?

A: Famotidine API is supplied as a white or yellowish-white crystalline powder. This physical form facilitates easy mixing and precise dosing during pharmaceutical manufacturing.

Q: How is the quality of Famotidine API maintained throughout its shelf life?

A: Proper storage in closed containers away from moisture and direct sunlight, as well as adherence to recommended handling procedures, help maintain its quality and effectiveness for up to five years.

Q: What is the process for integrating Famotidine API into pharmaceutical formulations?

A: Manufacturers dissolve or blend the crystalline powder with other excipients following strict pharmaceutical protocols, ensuring uniform dispersion and accurate dosage in the final drug product.

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