Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
01 1Bachem AG
02 1Apicore Pharmaceuticals Private Limited
03 1Azico Biophore India Private Limited
04 1MSN Life Sciences Private Limited
01 1SINCALIDE
02 2Sincalide
03 1sincalide
01 3India
02 1Switzerland
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
NDC Package Code : 55463-0004
Start Marketing Date : 1999-10-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42973-235
Start Marketing Date : 2017-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69575-4029
Start Marketing Date : 2018-12-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1000g/1000g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69766-102
Start Marketing Date : 2021-10-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Sincalide 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 Sincalide manufacturer or Sincalide supplier for your needs.
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A Kinevac manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Kinevac, including repackagers and relabelers. The FDA regulates Kinevac manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Kinevac 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 Kinevac supplier is an individual or a company that provides Kinevac active pharmaceutical ingredient (API) or Kinevac finished formulations upon request. The Kinevac suppliers may include Kinevac 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 Kinevac as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Kinevac 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 Kinevac 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 Kinevac and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Kinevac NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Kinevac suppliers with NDC on PharmaCompass.
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