Product NDC: | 0781-3074 |
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) |
Product NDC: | 0781-3074 |
Labeler Name: | Sandoz Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040615 |
Marketing Category: | ANDA |
Start Marketing Date: | 20060810 |
Package NDC: | 0781-3074-70 |
Package Description: | 1 VIAL, MULTI-DOSE in 1 CARTON (0781-3074-70) > 10 mL in 1 VIAL, MULTI-DOSE |
NDC Code | 0781-3074-70 |
Proprietary Name | Testosterone Cypionate |
Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (0781-3074-70) > 10 mL in 1 VIAL, MULTI-DOSE |
Product NDC | 0781-3074 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Testosterone Cypionate |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAMUSCULAR |
Start Marketing Date | 20060810 |
Marketing Category Name | ANDA |
Labeler Name | Sandoz Inc |
Substance Name | TESTOSTERONE CYPIONATE |
Strength Number | 200 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Androgen [EPC],Androgen Receptor Agonists [MoA],Androstanes [Chemical/Ingredient] |