Oxandrolone (Upsher-Smith Laboratories, LLC)
Welcome to the PulseAid listing for the Oxandrolone drug offered from Upsher-Smith Laboratories, LLC. This 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: | Upsher-Smith Laboratories, LLC |
| NON-PROPRIETARY NAME: | Oxandrolone |
| SUBSTANCE NAME: | OXANDROLONE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2006-12-01 |
| END MARKETING DATE: | 0000-00-00 |
Oxandrolone HUMAN PRESCRIPTION DRUG Details:
| Item Description | Oxandrolone from Upsher-Smith Laboratories, LLC |
| LABELER NAME: | Upsher-Smith Laboratories, LLC |
| DEA SCHEDULE: | CIII
|
| ACTIVE STRENGTH: | 2.5(mg/1) |
| START MARKETING DATE: | 2006-12-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0245-0271_24672ff6-88f0-4cb5-95c0-12d9907534f5 |
| PRODUCT NDC: | 0245-0271 |
| APPLICATION NUMBER: | ANDA076761 |
Other OXANDROLONE Pharmaceutical Manufacturers / Labelers:
