Product Description
Pyrantel Pamoate USP API is an anthelmintic pharmaceutical active ingredient, usually appearing as a yellow-to-tan, water-insoluble solid
. It treats intestinal parasitic infections pinworm, hookworm by causing neuromuscular paralysis in worms. Superior Pharmaceutical QualityPyrantel Pamoate USP API is meticulously manufactured to meet international pharmacopoeial standards such as USP, BP, EP, and IP. Its assay, purity, and microbial count parameters are rigorously monitored, ensuring a premium-quality, stable ingredient for pharmaceutical production. The product is practically tasteless and odorless, providing versatility in various formulations.
Applications and UsageWidely used as an anthelmintic, Pyrantel Pamoate USP API serves as the principal ingredient in medications designed to combat intestinal worm infections. Its favorable solubility profile and compliance with established purity standards guarantee safety and efficacy, making it a preferred choice among pharmaceutical companies, exporters, and healthcare providers.
Packaging and Storage SolutionsTo maintain product integrity, Pyrantel Pamoate USP API is packaged in secure HDPE drums lined with double polyethylene bags, typically in 25 kg quantities. Recommended storage at room temperature ensures stability and preserves its five-year shelf life. The packaging method is optimized for safe transport and ease of handling in both domestic and international markets.
FAQ's of Pyrantel Pamoate USP API:
Q: How is Pyrantel Pamoate USP API identified and qualified for pharmaceutical use?
A: Pyrantel Pamoate USP API is identified according to the United States Pharmacopeia (USP) standards and undergoes thorough testing for assay, purity, related substances, and microbial limits. It also complies with ICH Q3C guidelines for residual solvents, ensuring it is safe and effective for pharmaceutical manufacturing.
Q: What are the main applications of Pyrantel Pamoate USP API?
A: This API is predominantly used in the formulation of medicines targeting intestinal worm infections. Its anthelmintic properties make it essential for producing safe and effective antiparasitic drugs widely supplied to healthcare providers.
Q: Where is Pyrantel Pamoate USP API manufactured and supplied from?
A: The product is manufactured, supplied, and distributed in India, serving both domestic and international markets through a network involving exporters, suppliers, traders, and wholesalers.
Q: What is the recommended storage process for maintaining Pyrantel Pamoate USP API's stability?
A: The API should be stored at room temperature in its original packaging-HDPE drums with double polyethylene bags-to preserve its chemical stability and extend shelf life up to five years.
Q: How does Pyrantel Pamoate USP API benefit pharmaceutical manufacturers?
A: Manufacturers benefit from its high purity (98%+), consistent particle size, excellent stability, and compliance with global pharmacopoeial standards. These characteristics simplify formulation, ensure safety, and facilitate regulatory approval.
Q: When does the shelf life of Pyrantel Pamoate USP API expire under proper storage?
A: Provided it is kept in recommended storage conditions and unopened packaging, Pyrantel Pamoate USP API retains its efficacy and quality for up to five years from the date of manufacture.
Q: What safety considerations are associated with the usage of Pyrantel Pamoate USP API?
A: The API is non-poisonous when used at therapeutic doses. It has a favorable safety profile with very low levels of heavy metals and complies with strict microbial and residual solvent requirements, making it suitable for pharmaceutical use.