Aspen API. More than just an API.
01 1Aspen Oss B.V.
02 1Curia Spain S.A.U.
03 1Gedeon Richter Plc.
04 2Industriale Chimica s.r.l.
05 1STERLING SPA
06 1Sterling S.p.A.
01 2ETONOGESTREL
02 5Etonogestrel
01 1Hungary
02 4Italy
03 1Netherlands
04 1U.S.A
Aspen API. More than just an API.
NDC Package Code : 60870-0475
Start Marketing Date : 2021-07-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65089-0053
Start Marketing Date : 2006-07-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 45541-1192
Start Marketing Date : 2010-01-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63190-0260
Start Marketing Date : 2001-10-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63190-0480
Start Marketing Date : 2001-10-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 64918-1500
Start Marketing Date : 2014-11-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 64918-1906
Start Marketing Date : 2019-11-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Etonogestrel manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Etonogestrel, including repackagers and relabelers. The FDA regulates Etonogestrel manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Etonogestrel 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 Etonogestrel manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Etonogestrel supplier is an individual or a company that provides Etonogestrel active pharmaceutical ingredient (API) or Etonogestrel finished formulations upon request. The Etonogestrel suppliers may include Etonogestrel API manufacturers, exporters, distributors and traders.
click here to find a list of Etonogestrel 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 Etonogestrel as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Etonogestrel 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 Etonogestrel 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 Etonogestrel and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Etonogestrel NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Etonogestrel suppliers with NDC on PharmaCompass.
We have 5 companies offering Etonogestrel
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