Mucinex DMaximum Strength (Reckitt Benckiser LLC)
Welcome to the PulseAid listing for the Mucinex D drug offered from Reckitt Benckiser LLC. 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: | Reckitt Benckiser LLC |
| 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: | 2012-06-26 |
| END MARKETING DATE: | 0000-00-00 |
Mucinex D Maximum Strength HUMAN OTC DRUG Details:
| Item Description | Mucinex D Maximum Strength from Reckitt Benckiser LLC |
| LABELER NAME: | Reckitt Benckiser LLC |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 1200; 120(mg/1; mg/1) |
| START MARKETING DATE: | 2012-06-26 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 63824-041_6185f4c5-985f-4013-bb17-0b712827364e |
| PRODUCT NDC: | 63824-041 |
| APPLICATION NUMBER: | NDA021585 |
Other GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
