Desonide (G&W Laboratories, Inc.)
Welcome to the PulseAid listing for the Desonide drug offered from G&W Laboratories, 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: | G&W Laboratories, Inc. |
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: | 2016-08-19 |
END MARKETING DATE: | 0000-00-00 |
Desonide HUMAN PRESCRIPTION DRUG Details:
Item Description | Desonide from G&W Laboratories, Inc. |
LABELER NAME: | G&W Laboratories, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 0.5(mg/g) |
START MARKETING DATE: | 2016-08-19 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0713-0661_90a1c83b-0258-2f4b-e740-8c81cc2916c7 |
PRODUCT NDC: | 0713-0661 |
APPLICATION NUMBER: | ANDA074027 |
Other DESONIDE Pharmaceutical Manufacturers / Labelers: