Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
01 2Bachem Americas, Inc.
02 1Ambiopharm, Inc.
03 1MSN Life Sciences Private Limited
04 1PolyPeptide Laboratories (Sweden) AB
05 1PolyPeptide Laboratories Private Limited
06 1PolyPeptide SA
07 1Resilience US, Inc.
08 1SpecGx LLC
01 1EXENATIDE
02 7Exenatide
03 1exenatide
01 1India
02 1Ireland
03 5Switzerland
04 1U.S.A
05 1Blank
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
NDC Package Code : 52416-105
Start Marketing Date : 2005-04-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
NDC Package Code : 52416-125
Start Marketing Date : 2021-08-31
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : EXPORT ONLY
NDC Package Code : 41524-0003
Start Marketing Date : 2012-09-06
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0406-7310
Start Marketing Date : 2013-11-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69766-078
Start Marketing Date : 2020-02-17
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63586-1469
Start Marketing Date : 2017-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (4000g/4000g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 68067-0397
Start Marketing Date : 2020-01-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1000g/1000g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59149-004
Start Marketing Date : 2023-02-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (250g/250g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 83516-0107
Start Marketing Date : 2023-01-31
End Marketing Date : 2026-06-30
Dosage Form (Strength) : POWDER (5mg/100mg)
Marketing Category : DRUG FOR FURTHER PROCESSING
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PharmaCompass offers a list of Exenatide 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 Exenatide manufacturer or Exenatide supplier for your needs.
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PharmaCompass also assists you with knowing the Exenatide API Price utilized in the formulation of products. Exenatide API Price is not always fixed or binding as the Exenatide Price is obtained through a variety of data sources. The Exenatide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Exenatide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Exenatide, including repackagers and relabelers. The FDA regulates Exenatide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Exenatide 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 Exenatide supplier is an individual or a company that provides Exenatide active pharmaceutical ingredient (API) or Exenatide finished formulations upon request. The Exenatide suppliers may include Exenatide 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 Exenatide as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Exenatide 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 Exenatide 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 Exenatide and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Exenatide NDC to their finished compounded human drug products, they may choose to do so.
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