01 1MSN Laboratories Private Limited
01 1Vismodegib
01 1India
NDC Package Code : 54893-0513
Start Marketing Date : 2025-02-28
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Vismodegib 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 Vismodegib manufacturer or Vismodegib supplier for your needs.
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A Hhantag691 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hhantag691, including repackagers and relabelers. The FDA regulates Hhantag691 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hhantag691 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Hhantag691 supplier is an individual or a company that provides Hhantag691 active pharmaceutical ingredient (API) or Hhantag691 finished formulations upon request. The Hhantag691 suppliers may include Hhantag691 API manufacturers, exporters, distributors and traders.
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National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Hhantag691 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Hhantag691 API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Hhantag691 as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Hhantag691 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Hhantag691 NDC to their finished compounded human drug products, they may choose to do so.
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