Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
01 1Bachem AG
01 1DASIGLUCAGON HYDROCHLORIDE
01 1Switzerland
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
NDC Package Code : 55463-0037
Start Marketing Date : 2021-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
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A GLUCAGON HYDROCHLORIDE RECOMBINANT manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of GLUCAGON HYDROCHLORIDE RECOMBINANT, including repackagers and relabelers. The FDA regulates GLUCAGON HYDROCHLORIDE RECOMBINANT manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. GLUCAGON HYDROCHLORIDE RECOMBINANT 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 GLUCAGON HYDROCHLORIDE RECOMBINANT supplier is an individual or a company that provides GLUCAGON HYDROCHLORIDE RECOMBINANT active pharmaceutical ingredient (API) or GLUCAGON HYDROCHLORIDE RECOMBINANT finished formulations upon request. The GLUCAGON HYDROCHLORIDE RECOMBINANT suppliers may include GLUCAGON HYDROCHLORIDE RECOMBINANT 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 GLUCAGON HYDROCHLORIDE RECOMBINANT as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for GLUCAGON HYDROCHLORIDE RECOMBINANT 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 GLUCAGON HYDROCHLORIDE RECOMBINANT 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 GLUCAGON HYDROCHLORIDE RECOMBINANT and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a GLUCAGON HYDROCHLORIDE RECOMBINANT NDC to their finished compounded human drug products, they may choose to do so.
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