Ultravate (Ranbaxy Laboratories, Inc.)
Welcome to the PulseAid listing for the Ultravate drug offered from Ranbaxy 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: | Ranbaxy Laboratories, Inc. |
NON-PROPRIETARY NAME: | halobetasol propionate |
SUBSTANCE NAME: | HALOBETASOL PROPIONATE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
ROUTE: | TOPICAL |
DOSAGE FORM: | LOTION |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2016-03-01 |
END MARKETING DATE: | 0000-00-00 |
Ultravate HUMAN PRESCRIPTION DRUG Details:
Item Description | Ultravate from Ranbaxy Laboratories, Inc. |
LABELER NAME: | Ranbaxy Laboratories, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 0.5(mg/g) |
START MARKETING DATE: | 2016-03-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 10631-122_1e0e23af-03ba-4520-ab13-7544e0c6a7f1 |
PRODUCT NDC: | 10631-122 |
APPLICATION NUMBER: | NDA208183 |
Other HALOBETASOL PROPIONATE Pharmaceutical Manufacturers / Labelers: