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Testosterone Cypionate - 0574-0820-01 - (Testosterone Cypionate)

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Drug Information of Testosterone Cypionate

Product NDC: 0574-0820
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: 0574-0820
Labeler Name: Paddock Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040530
Marketing Category: ANDA
Start Marketing Date: 20091221

Package Information of Testosterone Cypionate

Package NDC: 0574-0820-01
Package Description: 1 VIAL in 1 CARTON (0574-0820-01) > 1 mL in 1 VIAL

NDC Information of Testosterone Cypionate

NDC Code 0574-0820-01
Proprietary Name Testosterone Cypionate
Package Description 1 VIAL in 1 CARTON (0574-0820-01) > 1 mL in 1 VIAL
Product NDC 0574-0820
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Testosterone Cypionate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR
Start Marketing Date 20091221
Marketing Category Name ANDA
Labeler Name Paddock Laboratories, Inc.
Substance Name TESTOSTERONE CYPIONATE
Strength Number 200
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Testosterone Cypionate


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