Mucinex D (REMEDYREPACK INC.)
Welcome to the PulseAid listing for the Mucinex D drug offered from REMEDYREPACK INC.. This pharmaceutical is classified as a HUMAN OTC 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 OTC DRUG drug type category.
| LABELER NAME / MANUFACTURER: | REMEDYREPACK INC. |
| NON-PROPRIETARY NAME: | Guaifenesin and Pseudoephedrine Hydrochloride |
| SUBSTANCE NAME: | GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET, EXTENDED RELEASE |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 2017-05-11 |
| END MARKETING DATE: | 0000-00-00 |
Mucinex D HUMAN OTC DRUG Details:
| Item Description | Mucinex D from REMEDYREPACK INC. |
| LABELER NAME: | REMEDYREPACK INC. |
| DEA SCHEDULE: |
|
| ACTIVE STRENGTH: | 600; 60(mg/1; mg/1) |
| START MARKETING DATE: | 2017-05-11 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 70518-0523_4f4872a4-2a54-232b-e054-00144ff88e88 |
| PRODUCT NDC: | 70518-0523 |
| APPLICATION NUMBER: | NDA021585 |
Other GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
