PROMETHAZINE DM (REMEDYREPACK INC.)
Welcome to the PulseAid listing for the PROMETHAZINE DM drug offered from REMEDYREPACK INC.. This Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC],Sigma-1 Agonist [EPC],Uncompetitive NMDA Receptor Antagonists [MoA],Sigma-1 Receptor Agonists [MoA],Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] 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: | REMEDYREPACK INC. |
NON-PROPRIETARY NAME: | Dextromethorphan Hydrobromide and Promethazine Hydrochloride |
SUBSTANCE NAME: | DEXTROMETHORPHAN HYDROBROMIDE; PROMETHAZINE HYDROCHLORIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC],Sigma-1 Agonist [EPC],Uncompetitive NMDA Receptor Antagonists [MoA],Sigma-1 Receptor Agonists [MoA],Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
ROUTE: | ORAL |
DOSAGE FORM: | SOLUTION |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2017-04-11 |
END MARKETING DATE: | 0000-00-00 |
PROMETHAZINE DM HUMAN PRESCRIPTION DRUG Details:
Item Description | PROMETHAZINE DM from REMEDYREPACK INC. |
LABELER NAME: | REMEDYREPACK INC. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 15; 6.25(mg/5mL; mg/5mL) |
START MARKETING DATE: | 2017-04-11 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 70518-0418_513e911a-e13b-336c-e054-00144ff8d46c |
PRODUCT NDC: | 70518-0418 |
APPLICATION NUMBER: | ANDA040649 |
Other DEXTROMETHORPHAN HYDROBROMIDE; PROMETHAZINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: