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Depo-Testosterone
Depo-Testosterone - 0009-0417-01 - (testosterone cypionate)
Drug Information of Depo-Testosterone
| Product NDC: | 0009-0417 |
| 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: | 0009-0417 |
| Labeler Name: | Pharmacia and Upjohn Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA085635 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19790725 |
Package Information of Depo-Testosterone
| Package NDC: | 0009-0417-01 |
| Package Description: | 1 mL in 1 VIAL (0009-0417-01) |
NDC Information of Depo-Testosterone
| NDC Code | 0009-0417-01 |
| Proprietary Name | Depo-Testosterone |
| Package Description | 1 mL in 1 VIAL (0009-0417-01) |
| Product NDC | 0009-0417 |
| 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 | 200 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Androgen [EPC],Androgen Receptor Agonists [MoA],Androstanes [Chemical/Ingredient] |
