G-P-TUSS DXP (Kramer Novis)


Welcome to the PulseAid listing for the G-P-TUSS DXP drug offered from Kramer Novis. 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: Kramer Novis
NON-PROPRIETARY NAME: dexbrompheniramine, dextromethorphan, and phenylephrine
SUBSTANCE NAME: DEXBROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: SYRUP
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2013-01-24
END MARKETING DATE: 0000-00-00


G-P-TUSS DXP HUMAN OTC DRUG Details:

Item DescriptionG-P-TUSS DXP from Kramer Novis
LABELER NAME: Kramer Novis
DEA SCHEDULE:
ACTIVE STRENGTH: 2; 20; 10(mg/5mL; mg/5mL; mg/5mL)
START MARKETING DATE: 2013-01-24
END MARKETING DATE: 0000-00-00
PRODUCT ID: 52083-602_cd027353-8669-4aac-b94f-d2ceb7456ef4
PRODUCT NDC: 52083-602
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