01 1Asymchem Laboratories (Tianjin) Co., Ltd.
01 1Taletrectinib Adipate
01 1Blank
NDC Package Code : 72015-007
Start Marketing Date : 2025-06-13
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 Taletrectinib 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 Taletrectinib manufacturer or Taletrectinib supplier for your needs.
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A Taletrectinib adipate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Taletrectinib adipate, including repackagers and relabelers. The FDA regulates Taletrectinib adipate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Taletrectinib adipate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Taletrectinib adipate supplier is an individual or a company that provides Taletrectinib adipate active pharmaceutical ingredient (API) or Taletrectinib adipate finished formulations upon request. The Taletrectinib adipate suppliers may include Taletrectinib adipate 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 Taletrectinib adipate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Taletrectinib adipate 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 Taletrectinib adipate 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 Taletrectinib adipate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Taletrectinib adipate NDC to their finished compounded human drug products, they may choose to do so.
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