Product NDC: | 54868-3618 |
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: | 54868-3618 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040530 |
Marketing Category: | ANDA |
Start Marketing Date: | 20070810 |
Package NDC: | 54868-3618-1 |
Package Description: | 1 VIAL in 1 CARTON (54868-3618-1) > 1 mL in 1 VIAL |
NDC Code | 54868-3618-1 |
Proprietary Name | Testosterone Cypionate |
Package Description | 1 VIAL in 1 CARTON (54868-3618-1) > 1 mL in 1 VIAL |
Product NDC | 54868-3618 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Testosterone Cypionate |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAMUSCULAR |
Start Marketing Date | 20070810 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | TESTOSTERONE CYPIONATE |
Strength Number | 200 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Androgen [EPC],Androgen Receptor Agonists [MoA],Androstanes [Chemical/Ingredient] |