Desonide (Glenmark Pharmaceuticals Inc., USA)
Welcome to the PulseAid listing for the Desonide drug offered from Glenmark Pharmaceuticals Inc., USA. 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: | Glenmark Pharmaceuticals Inc., USA |
NON-PROPRIETARY NAME: | Desonide |
SUBSTANCE NAME: | DESONIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
ROUTE: | TOPICAL |
DOSAGE FORM: | CREAM |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2017-07-24 |
END MARKETING DATE: | 0000-00-00 |
Desonide HUMAN PRESCRIPTION DRUG Details:
Item Description | Desonide from Glenmark Pharmaceuticals Inc., USA |
LABELER NAME: | Glenmark Pharmaceuticals Inc., USA |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 0.5(mg/g) |
START MARKETING DATE: | 2017-07-24 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 68462-252_12741be9-593f-460b-8e53-1493df143dca |
PRODUCT NDC: | 68462-252 |
APPLICATION NUMBER: | ANDA209729 |
Other DESONIDE Pharmaceutical Manufacturers / Labelers: