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Depo-Testosterone - 54868-0216-1 - (testosterone cypionate)

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Drug Information of Depo-Testosterone

Product NDC: 54868-0216
Proprietary Name: Depo-Testosterone
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 Depo-Testosterone

Product NDC: 54868-0216
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA085635
Marketing Category: ANDA
Start Marketing Date: 19940712

Package Information of Depo-Testosterone

Package NDC: 54868-0216-1
Package Description: 1 VIAL in 1 CARTON (54868-0216-1) > 1 mL in 1 VIAL

NDC Information of Depo-Testosterone

NDC Code 54868-0216-1
Proprietary Name Depo-Testosterone
Package Description 1 VIAL in 1 CARTON (54868-0216-1) > 1 mL in 1 VIAL
Product NDC 54868-0216
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name testosterone cypionate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR
Start Marketing Date 19940712
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
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 Depo-Testosterone


General Information