Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
NDC Package Code : 55463-0024
Start Marketing Date : 2004-03-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Buserelin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Buserelin, including repackagers and relabelers. The FDA regulates Buserelin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Buserelin API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Buserelin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Buserelin supplier is an individual or a company that provides Buserelin active pharmaceutical ingredient (API) or Buserelin finished formulations upon request. The Buserelin suppliers may include Buserelin API manufacturers, exporters, distributors and traders.
click here to find a list of Buserelin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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 Buserelin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Buserelin 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 Buserelin 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 Buserelin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Buserelin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Buserelin suppliers with NDC on PharmaCompass.
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