Prednisolone (Teva Pharmaceuticals USA, Inc.)
Welcome to the PulseAid listing for the Prednisolone drug offered from Teva Pharmaceuticals USA, Inc.. This Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] 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: | Teva Pharmaceuticals USA, Inc. |
NON-PROPRIETARY NAME: | Prednisolone |
SUBSTANCE NAME: | PREDNISOLONE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
ROUTE: | ORAL |
DOSAGE FORM: | SOLUTION |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 1998-12-11 |
END MARKETING DATE: | 2018-02-28 |
Prednisolone HUMAN PRESCRIPTION DRUG Details:
Item Description | Prednisolone from Teva Pharmaceuticals USA, Inc. |
LABELER NAME: | Teva Pharmaceuticals USA, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 15(mg/5mL) |
START MARKETING DATE: | 1998-12-11 |
END MARKETING DATE: | 2018-02-28 |
PRODUCT ID: | 0093-6118_51806556-6892-450f-911c-84182e9e34a7 |
PRODUCT NDC: | 0093-6118 |
APPLICATION NUMBER: | ANDA089081 |
Other PREDNISOLONE Pharmaceutical Manufacturers / Labelers: