Aspen API. More than just an API.
01 1Aspen Oss B.V.
02 1Symbiotec Pharmalab Private Limited
03 1Farmabios S.p.A.
04 1ASG Biochem Pvt. LTD
05 1Curia Spain S.A.U.
06 1F.I.S. FABBRICA ITALIANA SINTETICI S.P.A.
07 1Fagron Inc
08 1Jiangsu Jiaerke Pharmaceuticals Group Corp., Ltd
09 1Jiangsu Jiaerke Pharmaceuticals Group Corp., Ltd.
10 1LETCO MEDICAL, LLC
11 1Medisca Inc.
12 1Pharma Source Direct, Inc.
13 1Pharmacia and Upjohn Company LLC
14 1Professional Compounding Centers of America
15 1Professional Compounding Centers of America dba PCCA
16 1SHAKTI LIFESCIENCE PRIVATE LIMITED
17 1Trifarma S.p.A.
18 1zhejiang xianju pharmaceutical co., Ltd.
01 4TESTOSTERONE CYPIONATE
02 14Testosterone Cypionate
01 3China
02 1Germany
03 3India
04 2Italy
05 2Netherlands
06 5U.S.A
07 2United Kingdom
NDC Package Code : 60870-0252
Start Marketing Date : 1999-06-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 22552-0010
Start Marketing Date : 2010-04-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46439-8736
Start Marketing Date : 2011-05-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 43647-678
Start Marketing Date : 2015-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48087-0096
Start Marketing Date : 2010-12-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51552-0104
Start Marketing Date : 1998-04-01
End Marketing Date : 2025-04-26
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 38779-0164
Start Marketing Date : 2014-06-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-0189
Start Marketing Date : 1999-07-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 0009-0027
Start Marketing Date : 2014-07-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46204-0371
Start Marketing Date : 2019-09-02
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Testosterone Cypionate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Testosterone Cypionate, including repackagers and relabelers. The FDA regulates Testosterone Cypionate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Testosterone 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 Testosterone Cypionate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Testosterone Cypionate supplier is an individual or a company that provides Testosterone Cypionate active pharmaceutical ingredient (API) or Testosterone Cypionate finished formulations upon request. The Testosterone Cypionate suppliers may include Testosterone Cypionate API manufacturers, exporters, distributors and traders.
click here to find a list of Testosterone Cypionate 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 Testosterone Cypionate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Testosterone 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 Testosterone 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 Testosterone Cypionate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Testosterone Cypionate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Testosterone Cypionate suppliers with NDC on PharmaCompass.
We have 16 companies offering Testosterone Cypionate
Get in contact with the supplier of your choice:
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