PRAMOSONE (Ferndale Laboratories, Inc.)
Welcome to the PulseAid listing for the PRAMOSONE drug offered from Ferndale 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: | Ferndale Laboratories, Inc. |
NON-PROPRIETARY NAME: | hydrocortisone acetate and pramoxine hydrochloride |
SUBSTANCE NAME: | HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
ROUTE: | TOPICAL |
DOSAGE FORM: | OINTMENT |
MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
START MARKETING DATE: | 1989-07-21 |
END MARKETING DATE: | 2017-12-31 |
PRAMOSONE HUMAN PRESCRIPTION DRUG Details:
Item Description | PRAMOSONE from Ferndale Laboratories, Inc. |
LABELER NAME: | Ferndale Laboratories, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 25; 10(mg/g; mg/g) |
START MARKETING DATE: | 1989-07-21 |
END MARKETING DATE: | 2017-12-31 |
PRODUCT ID: | 0496-0777_333d1ee2-97b9-4266-897f-1c3ac2e620d6 |
PRODUCT NDC: | 0496-0777 |
APPLICATION NUMBER: | |
Other HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: