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Testosterone Cypionate
Testosterone Cypionate - 62756-016-40 - (Testosterone Cypionate)
Drug Information of Testosterone Cypionate
| Product NDC: | 62756-016 |
| 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) |
Labeler Information of Testosterone Cypionate
| Product NDC: | 62756-016 |
| Labeler Name: | Sun Pharmaceutical Industries Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA201720 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130617 |
Package Information of Testosterone Cypionate
| Package NDC: | 62756-016-40 |
| Package Description: | 1 VIAL, MULTI-DOSE in 1 CARTON (62756-016-40) > 10 mL in 1 VIAL, MULTI-DOSE |
NDC Information of Testosterone Cypionate
| NDC Code | 62756-016-40 |
| Proprietary Name | Testosterone Cypionate |
| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (62756-016-40) > 10 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 62756-016 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Testosterone Cypionate |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 20130617 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharmaceutical Industries Limited |
| Substance Name | TESTOSTERONE CYPIONATE |
| Strength Number | 200 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Androgen [EPC],Androgen Receptor Agonists [MoA],Androstanes [Chemical/Ingredient] |
