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Testosterone Cypionate - 62756-015-40 - (Testosterone Cypionate)

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Drug Information of Testosterone Cypionate

Product NDC: 62756-015
Proprietary Name: Testosterone Cypionate
Non Proprietary Name: Testosterone Cypionate
Active Ingredient(s): 200    mg/mL & nbsp;   Testosterone Cypionate
Administration Route(s): INTRAMUSCULAR
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Testosterone Cypionate

Product NDC: 62756-015
Labeler Name: Sun Pharmaceutical Industries Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201720
Marketing Category: ANDA
Start Marketing Date: 20130617

Package Information of Testosterone Cypionate

Package NDC: 62756-015-40
Package Description: 1 VIAL in 1 CARTON (62756-015-40) > 1 mL in 1 VIAL

NDC Information of Testosterone Cypionate

NDC Code 62756-015-40
Proprietary Name Testosterone Cypionate
Package Description 1 VIAL in 1 CARTON (62756-015-40) > 1 mL in 1 VIAL
Product NDC 62756-015
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Testosterone Cypionate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR
Start Marketing Date 20130617
Marketing Category Name ANDA
Labeler Name Sun Pharmaceutical Industries Limited
Substance Name TESTOSTERONE CYPIONATE
Strength Number 200
Strength Unit mg/mL
Pharmaceutical Classes Androgen [EPC],Androgen Receptor Agonists [MoA],Androstanes [Chemical/Ingredient]

Complete Information of Testosterone Cypionate


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