PrednisoLONE (Qualitest Pharmaceuticals)
Welcome to the PulseAid listing for the PrednisoLONE drug offered from Qualitest Pharmaceuticals. 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: | Qualitest Pharmaceuticals |
NON-PROPRIETARY NAME: | Prednisolone |
SUBSTANCE NAME: | PREDNISOLONE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
ROUTE: | ORAL |
DOSAGE FORM: | SYRUP |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2007-09-21 |
END MARKETING DATE: | 0000-00-00 |
PrednisoLONE HUMAN PRESCRIPTION DRUG Details:
Item Description | PrednisoLONE from Qualitest Pharmaceuticals |
LABELER NAME: | Qualitest Pharmaceuticals |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 15(mg/5mL) |
START MARKETING DATE: | 2007-09-21 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0603-1567_318f21d5-6414-4804-ae2f-d97de6cfde6a |
PRODUCT NDC: | 0603-1567 |
APPLICATION NUMBER: | ANDA040775 |
Other PREDNISOLONE Pharmaceutical Manufacturers / Labelers: