01 1Peace of Mind Pharmaceuticals LLC
01 1Thiopental
01 1U.S.A
NDC Package Code : 72735-020
Start Marketing Date : 2020-09-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (250g/250g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
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PharmaCompass offers a list of Thiopental Sodium 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 Thiopental Sodium manufacturer or Thiopental Sodium supplier for your needs.
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A Tiobarbital Braun manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tiobarbital Braun, including repackagers and relabelers. The FDA regulates Tiobarbital Braun manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tiobarbital Braun 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 Tiobarbital Braun supplier is an individual or a company that provides Tiobarbital Braun active pharmaceutical ingredient (API) or Tiobarbital Braun finished formulations upon request. The Tiobarbital Braun suppliers may include Tiobarbital Braun 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 Tiobarbital Braun as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Tiobarbital Braun 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 Tiobarbital Braun 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 Tiobarbital Braun and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tiobarbital Braun NDC to their finished compounded human drug products, they may choose to do so.
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