ED BRON GP (EDWARDS PHARMACEUTICALS, INC.)
Welcome to the PulseAid listing for the ED BRON GP drug offered from EDWARDS PHARMACEUTICALS, 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: | EDWARDS PHARMACEUTICALS, INC. |
NON-PROPRIETARY NAME: | GUAIFENESIN and PHENYLEPHRINE |
SUBSTANCE NAME: | GUAIFENESIN; PHENYLEPHRINE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | LIQUID |
MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
START MARKETING DATE: | 2012-06-01 |
END MARKETING DATE: | 0000-00-00 |
ED BRON GP HUMAN OTC DRUG Details:
Item Description | ED BRON GP from EDWARDS PHARMACEUTICALS, INC. |
LABELER NAME: | EDWARDS PHARMACEUTICALS, INC. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 100; 5(mg/5mL; mg/5mL) |
START MARKETING DATE: | 2012-06-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0485-0208_fea45bff-6e84-492c-b9f0-eae03248536f |
PRODUCT NDC: | 0485-0208 |
APPLICATION NUMBER: | part341 |
Other GUAIFENESIN; PHENYLEPHRINE Pharmaceutical Manufacturers / Labelers: