Vanapain PM (GM Pharmaceuticals, Inc.)


Welcome to the PulseAid listing for the Vanapain PM drug offered from GM 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: GM Pharmaceuticals, Inc.
NON-PROPRIETARY NAME: Choline Salicylate, Diphenhydramine Hydrochloride
SUBSTANCE NAME: CHOLINE SALICYLATE; DIPHENHYDRAMINE HYDROCHLORIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: LIQUID
MARKETING CATEGORY NAME: OTC MONOGRAPH NOT FINAL
START MARKETING DATE: 2013-10-28
END MARKETING DATE: 0000-00-00


Vanapain PM HUMAN OTC DRUG Details:

Item DescriptionVanapain PM from GM Pharmaceuticals, Inc.
LABELER NAME: GM Pharmaceuticals, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 870; 50(mg/57mL; mg/57mL)
START MARKETING DATE: 2013-10-28
END MARKETING DATE: 0000-00-00
PRODUCT ID: 58809-444_1edb4799-f2db-1737-e054-00144ff8d46c
PRODUCT NDC: 58809-444
APPLICATION NUMBER: part343

Other CHOLINE SALICYLATE; DIPHENHYDRAMINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
GM Pharmaceuticals, Inc.Vanapain PM