Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
01 1Symbiotec Pharmalab Private Limited
02 1Aspen Oss B.V.
03 1ASG Biochem Pvt. LTD.
04 2Bayer AG
05 1Curia Spain S.A.U.
06 2Industriale Chimica s.r.l.
07 1N.V. Organon
08 1Professional Compounding Centers of America
09 2Qinhuangdao Zizhu Pharmaceutical Co., Ltd.
10 1zhejiang xianju pharmaceutical co., Ltd.
01 3ETHINYL ESTRADIOL
02 6Ethinyl Estradiol
03 2Ethinylestradiol
04 1Ethinylestradiol Micronized
05 1ethinylestradiol
01 3China
02 2Germany
03 2India
04 2Italy
05 1Netherlands
06 2U.S.A
07 1United Kingdom
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
NDC Package Code : 22552-0034
Start Marketing Date : 2012-06-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Aspen API. More than just an API.
NDC Package Code : 60870-0463
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 : 43647-147
Start Marketing Date : 2023-08-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12866-1016
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 : 12866-1168
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 : 12860-0463
Start Marketing Date : 1980-04-25
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0305
Start Marketing Date : 2023-08-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 44132-002
Start Marketing Date : 2012-05-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 44132-010
Start Marketing Date : 2014-06-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 60722-3017
Start Marketing Date : 2022-10-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Ethinylestradiol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ethinylestradiol, including repackagers and relabelers. The FDA regulates Ethinylestradiol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ethinylestradiol 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 Ethinylestradiol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ethinylestradiol supplier is an individual or a company that provides Ethinylestradiol active pharmaceutical ingredient (API) or Ethinylestradiol finished formulations upon request. The Ethinylestradiol suppliers may include Ethinylestradiol API manufacturers, exporters, distributors and traders.
click here to find a list of Ethinylestradiol 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 Ethinylestradiol as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ethinylestradiol 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 Ethinylestradiol 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 Ethinylestradiol and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ethinylestradiol NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Ethinylestradiol suppliers with NDC on PharmaCompass.
We have 10 companies offering Ethinylestradiol
Get in contact with the supplier of your choice:
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