Fareva: One stop for innovative drug development, precision manufacturing and high-quality APIs.
01 1Valdepharm
02 160592
03 1AX Pharmaceutical Corp
04 1COHESION BIOTEC PRIVATE LIMITED
05 1DARMERICA, LLC
06 1Fagron Inc
07 1LETCO MEDICAL, LLC
08 1MORTAR & PESTLE
09 1SCH Global Services Private Limited
10 1SHAKTI LIFESCIENCE PRIVATE LIMITED
11 1Steroid S.p.A.
12 1zhejiang xianju pharmaceutical co., Ltd.
01 5ESTRADIOL CYPIONATE
02 6Estradiol Cypionate
03 1estradiol cypionate
01 1Canada
02 1China
03 3India
04 1Italy
05 1Luxembourg
06 1Netherlands
07 2U.S.A
08 2Blank
Fareva: One stop for innovative drug development, precision manufacturing and high-quality APIs.
NDC Package Code : 24823-916
Start Marketing Date : 2022-06-23
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 73377-071
Start Marketing Date : 2020-09-16
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 71052-277
Start Marketing Date : 2019-11-06
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (100g/100g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51552-1056
Start Marketing Date : 2004-09-01
End Marketing Date : 2026-09-29
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 62991-3212
Start Marketing Date : 2024-07-17
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 73774-003
Start Marketing Date : 2021-11-12
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49803-007
Start Marketing Date : 2019-01-21
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (25000g/25000g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 60722-3026
Start Marketing Date : 2025-11-13
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 60592-210
Start Marketing Date : 2019-11-24
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
NDC Package Code : 85207-016
Start Marketing Date : 2025-06-26
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (100g/100g)
Marketing Category : BULK INGREDIENT
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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PharmaCompass offers a list of Estradiol Cypionate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Estradiol Cypionate manufacturer or Estradiol Cypionate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Estradiol Cypionate manufacturer or Estradiol Cypionate supplier.
A Estradiol Cypionate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Estradiol Cypionate, including repackagers and relabelers. The FDA regulates Estradiol Cypionate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Estradiol Cypionate 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 Cypionate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Estradiol Cypionate supplier is an individual or a company that provides Estradiol Cypionate active pharmaceutical ingredient (API) or Estradiol Cypionate finished formulations upon request. The Estradiol Cypionate suppliers may include Estradiol Cypionate API manufacturers, exporters, distributors and traders.
click here to find a list of Estradiol Cypionate suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Cypionate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Estradiol Cypionate 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 Cypionate 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 Cypionate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Estradiol Cypionate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Estradiol Cypionate suppliers with NDC on PharmaCompass.
We have 10 companies offering Estradiol Cypionate
Get in contact with the supplier of your choice:
