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: