Guaifenesin and pseudoephedrine hydrochloride Extended Release (REMEDYREPACK INC.)
Welcome to the PulseAid listing for the Guaifenesin and pseudoephedrine hydrochloride Extended Release 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, pseudoephedrine hydrochloride |
| SUBSTANCE NAME: | GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET, EXTENDED RELEASE |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2016-11-21 |
| END MARKETING DATE: | 0000-00-00 |
Guaifenesin and pseudoephedrine hydrochloride Extended Release HUMAN OTC DRUG Details:
| Item Description | Guaifenesin and pseudoephedrine hydrochloride Extended Release from REMEDYREPACK INC. |
| LABELER NAME: | REMEDYREPACK INC. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 600; 60(mg/1; mg/1) |
| START MARKETING DATE: | 2016-11-21 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 70518-0011_41daf24d-4a93-0f9d-e054-00144ff8d46c |
| PRODUCT NDC: | 70518-0011 |
| APPLICATION NUMBER: | ANDA091071 |
Other GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
