BionatussDXP (Advanced Generic Corporation)


Welcome to the PulseAid listing for the Bionatuss drug offered from Advanced Generic Corporation. 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: Advanced Generic Corporation
NON-PROPRIETARY NAME: Dexbrompheniramine Maleate, Dextromethorphan, Phenylephrine
SUBSTANCE NAME: DEXBROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: LIQUID
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2009-10-01
END MARKETING DATE: 0000-00-00


Bionatuss DXP HUMAN OTC DRUG Details:

Item DescriptionBionatuss DXP from Advanced Generic Corporation
LABELER NAME: Advanced Generic Corporation
DEA SCHEDULE:
ACTIVE STRENGTH: 2; 20; 10(mg/5mL; mg/5mL; mg/5mL)
START MARKETING DATE: 2009-10-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 45737-210_3bf9cec4-9e30-44d2-b0d3-373167dbaddd
PRODUCT NDC: 45737-210
APPLICATION NUMBER: part341

Other DEXBROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Advanced Generic CorporationBionatuss
Kramer NovisSUPRESS A
Poly Pharmaceuticals, Inc.Alahist CF
Seyer Pharmatec, Inc.Panatuss