Aspen API. More than just an API.
01 1Aspen Oss B.V.
02 1ASG Biochem Pvt. LTD
03 1AX Pharmaceutical Corp
04 1Bayer AG
05 1Professional Compounding Centers of America dba PCCA
06 1SHAKTI LIFESCIENCE PRIVATE LIMITED
07 1Steroid S.p.A.
08 2Valdepharm
09 1zhejiang xianju pharmaceutical co., Ltd.
01 1ESTRADIOL VALERATE
02 6Estradiol Valerate
03 1Estradiol valerate
04 1Estradiol valerate micronized fine grade
05 1estradiol valerate
01 1Canada
02 1China
03 1Germany
04 2India
05 1Italy
06 2Luxembourg
07 1Netherlands
08 1United Kingdom
Aspen API. More than just an API.
NDC Package Code : 60870-0276
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 : 43647-145
Start Marketing Date : 2021-05-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 73377-063
Start Marketing Date : 2020-08-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 12866-1008
Start Marketing Date : 2017-05-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 24823-905
Start Marketing Date : 2010-02-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 24823-906
Start Marketing Date : 2011-04-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0076
Start Marketing Date : 2020-04-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 73774-004
Start Marketing Date : 2022-03-10
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49803-013
Start Marketing Date : 2024-02-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25000g/25000g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 60722-3022
Start Marketing Date : 2023-12-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Estradiol Valerate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Estradiol Valerate, including repackagers and relabelers. The FDA regulates Estradiol Valerate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Estradiol Valerate 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 Estradiol Valerate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Estradiol Valerate supplier is an individual or a company that provides Estradiol Valerate active pharmaceutical ingredient (API) or Estradiol Valerate finished formulations upon request. The Estradiol Valerate suppliers may include Estradiol Valerate API manufacturers, exporters, distributors and traders.
click here to find a list of Estradiol Valerate 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 Estradiol Valerate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Estradiol Valerate 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 Estradiol Valerate 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 Estradiol Valerate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Estradiol Valerate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Estradiol Valerate suppliers with NDC on PharmaCompass.
We have 9 companies offering Estradiol Valerate
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