Oxazepam (Sandoz Inc)
Welcome to the PulseAid listing for the Oxazepam drug offered from Sandoz Inc. This Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] 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: | Sandoz Inc |
| NON-PROPRIETARY NAME: | Oxazepam |
| SUBSTANCE NAME: | OXAZEPAM |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
| ROUTE: | ORAL |
| DOSAGE FORM: | CAPSULE |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 1988-04-19 |
| END MARKETING DATE: | 2019-08-31 |
Oxazepam HUMAN PRESCRIPTION DRUG Details:
| Item Description | Oxazepam from Sandoz Inc |
| LABELER NAME: | Sandoz Inc |
| DEA SCHEDULE: | CIV
|
| ACTIVE STRENGTH: | 10(mg/1) |
| START MARKETING DATE: | 1988-04-19 |
| END MARKETING DATE: | 2019-08-31 |
| PRODUCT ID: | 0781-2809_bf271f49-af20-4edd-a0d6-f1555b59dbb9 |
| PRODUCT NDC: | 0781-2809 |
| APPLICATION NUMBER: | ANDA071813 |
Other OXAZEPAM Pharmaceutical Manufacturers / Labelers:
