| Product NDC: | 0143-9726 |
| 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 |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0143-9726 |
| Labeler Name: | West-ward Pharmaceutical Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091244 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120501 |
| Package NDC: | 0143-9726-01 |
| Package Description: | 10 mL in 1 VIAL (0143-9726-01) |
| NDC Code | 0143-9726-01 |
| Proprietary Name | Testosterone Cypionate |
| Package Description | 10 mL in 1 VIAL (0143-9726-01) |
| Product NDC | 0143-9726 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Testosterone Cypionate |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 20120501 |
| Marketing Category Name | ANDA |
| Labeler Name | West-ward Pharmaceutical Corp |
| Substance Name | TESTOSTERONE CYPIONATE |
| Strength Number | 200 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Androgen [EPC],Androgen Receptor Agonists [MoA],Androstanes [Chemical/Ingredient] |