Aleve PM (Bayer HealthCare LLC.)


Welcome to the PulseAid listing for the Aleve PM drug offered from Bayer HealthCare LLC.. 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: Bayer HealthCare LLC.
NON-PROPRIETARY NAME: DIPHENHYDRAMINE HYDROCHLORIDE and NAPROXEN SODIUM
SUBSTANCE NAME: DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: TABLET, FILM COATED
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2014-09-09
END MARKETING DATE: 0000-00-00


Aleve PM HUMAN OTC DRUG Details:

Item DescriptionAleve PM from Bayer HealthCare LLC.
LABELER NAME: Bayer HealthCare LLC.
DEA SCHEDULE:
ACTIVE STRENGTH: 25; 220(mg/1; mg/1)
START MARKETING DATE: 2014-09-09
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0280-1200_55c4de2b-84b4-1497-e054-00144ff88e88
PRODUCT NDC: 0280-1200
APPLICATION NUMBER: NDA205352

Other DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Bayer HealthCare LLC.Aleve PM