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: