Product NDC: | 0009-0347 |
Proprietary Name: | Depo-Testosterone |
Non Proprietary Name: | testosterone cypionate |
Active Ingredient(s): | 100 mg/mL & nbsp; testosterone cypionate |
Administration Route(s): | INTRAMUSCULAR |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0009-0347 |
Labeler Name: | Pharmacia and Upjohn Company |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA085635 |
Marketing Category: | ANDA |
Start Marketing Date: | 19790725 |
Package NDC: | 0009-0347-02 |
Package Description: | 10 mL in 1 VIAL (0009-0347-02) |
NDC Code | 0009-0347-02 |
Proprietary Name | Depo-Testosterone |
Package Description | 10 mL in 1 VIAL (0009-0347-02) |
Product NDC | 0009-0347 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | testosterone cypionate |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAMUSCULAR |
Start Marketing Date | 19790725 |
Marketing Category Name | ANDA |
Labeler Name | Pharmacia and Upjohn Company |
Substance Name | TESTOSTERONE CYPIONATE |
Strength Number | 100 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Androgen [EPC],Androgen Receptor Agonists [MoA],Androstanes [Chemical/Ingredient] |