ALAHISTDMDM (Poly Pharmaceuticals, Inc.)


Welcome to the PulseAid listing for the ALAHISTDM drug offered from Poly 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: Poly Pharmaceuticals, Inc.
NON-PROPRIETARY NAME: Dexbrompheniramine Maleate, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride
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: 2016-09-01
END MARKETING DATE: 0000-00-00


ALAHISTDM DM HUMAN OTC DRUG Details:

Item DescriptionALAHISTDM DM from Poly Pharmaceuticals, Inc.
LABELER NAME: Poly Pharmaceuticals, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 2; 15; 7.5(mg/5mL; mg/5mL; mg/5mL)
START MARKETING DATE: 2016-09-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 50991-826_1073b5c0-9b6b-4485-b6a6-935742c6c865
PRODUCT NDC: 50991-826
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