Oxandrolone (Par Pharmaceutical, Inc.)
Welcome to the PulseAid listing for the Oxandrolone drug offered from Par Pharmaceutical, Inc.. 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: | Par Pharmaceutical, Inc. |
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: | 2007-08-20 |
END MARKETING DATE: | 0000-00-00 |
Oxandrolone HUMAN PRESCRIPTION DRUG Details:
Item Description | Oxandrolone from Par Pharmaceutical, Inc. |
LABELER NAME: | Par Pharmaceutical, Inc. |
DEA SCHEDULE: | CIII
|
ACTIVE STRENGTH: | 2.5(mg/1) |
START MARKETING DATE: | 2007-08-20 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 49884-301_b6abfdb5-35c6-4551-9af6-fc9ba287b310 |
PRODUCT NDC: | 49884-301 |
APPLICATION NUMBER: | ANDA077827 |
Other OXANDROLONE Pharmaceutical Manufacturers / Labelers: