EMVERM (Amedra Pharmaceuticals LLC)
Welcome to the PulseAid listing for the EMVERM drug offered from Amedra Pharmaceuticals LLC. This Antihelminthic [EPC] 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: | Amedra Pharmaceuticals LLC |
NON-PROPRIETARY NAME: | mebendazole |
SUBSTANCE NAME: | MEBENDAZOLE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Antihelminthic [EPC] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET, CHEWABLE |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2016-02-15 |
END MARKETING DATE: | 2018-11-30 |
EMVERM HUMAN PRESCRIPTION DRUG Details:
Item Description | EMVERM from Amedra Pharmaceuticals LLC |
LABELER NAME: | Amedra Pharmaceuticals LLC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 100(mg/1) |
START MARKETING DATE: | 2016-02-15 |
END MARKETING DATE: | 2018-11-30 |
PRODUCT ID: | 52054-107_1f128e35-5f96-45c1-ac0a-cf04ba9161c6 |
PRODUCT NDC: | 52054-107 |
APPLICATION NUMBER: | ANDA073580 |
Other MEBENDAZOLE Pharmaceutical Manufacturers / Labelers: