Product NDC: | 0517-0790 |
Proprietary Name: | Nandrolone Decanoate |
Non Proprietary Name: | Nandrolone Decanoate |
Active Ingredient(s): | 200 mg/mL & nbsp; Nandrolone Decanoate |
Administration Route(s): | INTRAMUSCULAR |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0517-0790 |
Labeler Name: | American Regent, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA091252 |
Marketing Category: | ANDA |
Start Marketing Date: | 20000101 |
Package NDC: | 0517-0790-20 |
Package Description: | 20 VIAL in 1 CARTON (0517-0790-20) > 1 mL in 1 VIAL |
NDC Code | 0517-0790-20 |
Proprietary Name | Nandrolone Decanoate |
Package Description | 20 VIAL in 1 CARTON (0517-0790-20) > 1 mL in 1 VIAL |
Product NDC | 0517-0790 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Nandrolone Decanoate |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAMUSCULAR |
Start Marketing Date | 20000101 |
Marketing Category Name | ANDA |
Labeler Name | American Regent, Inc. |
Substance Name | NANDROLONE DECANOATE |
Strength Number | 200 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Androgen [EPC] |