01 2BSV BioScience GmbH
02 1Instituto Massone S.A.
01 1MENOTROPINS
02 2Menotrophin
01 1Argentina
02 2Germany
NDC Package Code : 76403-4002
Start Marketing Date : 2017-12-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (2000000[iU]/2000000[iU])
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 76403-4001
Start Marketing Date : 2017-12-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1000000[iU]/1000000[iU])
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 67657-0004
Start Marketing Date : 2004-10-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Menotropins manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Menotropins, including repackagers and relabelers. The FDA regulates Menotropins manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Menotropins API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Menotropins supplier is an individual or a company that provides Menotropins active pharmaceutical ingredient (API) or Menotropins finished formulations upon request. The Menotropins suppliers may include Menotropins API manufacturers, exporters, distributors and traders.
click here to find a list of Menotropins 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 Menotropins as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Menotropins 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 Menotropins 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 Menotropins and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Menotropins NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Menotropins suppliers with NDC on PharmaCompass.
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