Aspen API. More than just an API.
01 1Aspen Oss B.V.
02 1Symbiotec Pharmalab Private Limited
01 1Ethynodiol Diacetate
02 1ethynodiol diacetate
01 1India
02 1Netherlands
NDC Package Code : 60870-0203
Start Marketing Date : 1980-04-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 22552-0031
Start Marketing Date : 2011-08-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Ethynodiol Diacetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ethynodiol Diacetate, including repackagers and relabelers. The FDA regulates Ethynodiol Diacetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ethynodiol Diacetate 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 Ethynodiol Diacetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ethynodiol Diacetate supplier is an individual or a company that provides Ethynodiol Diacetate active pharmaceutical ingredient (API) or Ethynodiol Diacetate finished formulations upon request. The Ethynodiol Diacetate suppliers may include Ethynodiol Diacetate API manufacturers, exporters, distributors and traders.
click here to find a list of Ethynodiol Diacetate 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 Ethynodiol Diacetate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ethynodiol Diacetate 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 Ethynodiol Diacetate 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 Ethynodiol Diacetate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ethynodiol Diacetate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Ethynodiol Diacetate suppliers with NDC on PharmaCompass.
We have 2 companies offering Ethynodiol Diacetate
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