Product NDC: | 67979-501 |
Proprietary Name: | DELATESTRYL |
Non Proprietary Name: | TESTOSTERONE ENANTHATE |
Active Ingredient(s): | 200 mg/mL & nbsp; TESTOSTERONE ENANTHATE |
Administration Route(s): | INTRAMUSCULAR |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67979-501 |
Labeler Name: | Endo Pharmaceuticals Solutions Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA009165 |
Marketing Category: | NDA |
Start Marketing Date: | 19531224 |
Package NDC: | 67979-501-40 |
Package Description: | 1 VIAL, MULTI-DOSE in 1 BOX (67979-501-40) > 5 mL in 1 VIAL, MULTI-DOSE |
NDC Code | 67979-501-40 |
Proprietary Name | DELATESTRYL |
Package Description | 1 VIAL, MULTI-DOSE in 1 BOX (67979-501-40) > 5 mL in 1 VIAL, MULTI-DOSE |
Product NDC | 67979-501 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | TESTOSTERONE ENANTHATE |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAMUSCULAR |
Start Marketing Date | 19531224 |
Marketing Category Name | NDA |
Labeler Name | Endo Pharmaceuticals Solutions Inc |
Substance Name | TESTOSTERONE ENANTHATE |
Strength Number | 200 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Androgen [EPC],Androgen Receptor Agonists [MoA],Androstanes [Chemical/Ingredient] |