01 1M/s Valens Molecules Private Limited
01 1Phenazopyridine Hydrochloride USP
01 1WC-0367
01 1India
Phenazopyridine Hydrochloride USP
Date of Issue : 2023-03-18
Valid Till : 2026-03-22
Written Confirmation Number : WC-0367
Address of the Firm : Unit-ll, Plot No23, Phase-1, IDA, Road No13, Jeedimetla, Medchal-Malkajgiri, 500...
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PharmaCompass offers a list of Phenazopyridine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Phenazopyridine manufacturer or Phenazopyridine supplier for your needs.
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PharmaCompass also assists you with knowing the Phenazopyridine API Price utilized in the formulation of products. Phenazopyridine API Price is not always fixed or binding as the Phenazopyridine Price is obtained through a variety of data sources. The Phenazopyridine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Bisteril manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bisteril, including repackagers and relabelers. The FDA regulates Bisteril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bisteril API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Bisteril manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Bisteril supplier is an individual or a company that provides Bisteril active pharmaceutical ingredient (API) or Bisteril finished formulations upon request. The Bisteril suppliers may include Bisteril API manufacturers, exporters, distributors and traders.
click here to find a list of Bisteril suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Bisteril written confirmation (Bisteril WC) is an official document issued by a regulatory agency to a Bisteril manufacturer, verifying that the manufacturing facility of a Bisteril active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Bisteril APIs or Bisteril finished pharmaceutical products to another nation, regulatory agencies frequently require a Bisteril WC (written confirmation) as part of the regulatory process.
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