Nandrolone Decanoate (American Regent, Inc.)
Welcome to the PulseAid listing for the Nandrolone Decanoate drug offered from American Regent, Inc.. This Androgen [EPC] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
| LABELER NAME / MANUFACTURER: | American Regent, Inc. |
| NON-PROPRIETARY NAME: | Nandrolone Decanoate |
| SUBSTANCE NAME: | NANDROLONE DECANOATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Androgen [EPC] |
| ROUTE: | INTRAMUSCULAR |
| DOSAGE FORM: | INJECTION, SOLUTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2000-01-01 |
| END MARKETING DATE: | 0000-00-00 |
Nandrolone Decanoate HUMAN PRESCRIPTION DRUG Details:
| Item Description | Nandrolone Decanoate from American Regent, Inc. |
| LABELER NAME: | American Regent, Inc. |
| DEA SCHEDULE: | CIII
|
| ACTIVE STRENGTH: | 200(mg/mL) |
| START MARKETING DATE: | 2000-01-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0517-0790_a5bf7ff6-bba0-4e86-92d1-9f929fd4794b |
| PRODUCT NDC: | 0517-0790 |
| APPLICATION NUMBER: | ANDA091252 |
Other NANDROLONE DECANOATE Pharmaceutical Manufacturers / Labelers: