Aspen API. More than just an API.
01 1Aspen Oss B.V.
02 1Instituto Massone S.A.
01 1CHORIONIC GONADOTROPIN
02 1Gonadorelin Diacetate Tetrahydrate
01 1Argentina
02 1Netherlands
GONADORELIN DIACETATE TETRAHYDRATE
NDC Package Code : 60870-0436
Start Marketing Date : 1999-01-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 67657-0005
Start Marketing Date : 1974-01-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Gonadorelin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gonadorelin, including repackagers and relabelers. The FDA regulates Gonadorelin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gonadorelin 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 Gonadorelin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Gonadorelin supplier is an individual or a company that provides Gonadorelin active pharmaceutical ingredient (API) or Gonadorelin finished formulations upon request. The Gonadorelin suppliers may include Gonadorelin API manufacturers, exporters, distributors and traders.
click here to find a list of Gonadorelin 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 Gonadorelin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Gonadorelin 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 Gonadorelin 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 Gonadorelin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Gonadorelin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Gonadorelin suppliers with NDC on PharmaCompass.
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