Bepreve (Bausch & Lomb Incorporated)


Welcome to the PulseAid listing for the Bepreve drug offered from Bausch & Lomb Incorporated. This Histamine-1 Receptor Antagonist [EPC] pharmaceutical is classified as a HUMAN PRESCRIPTION 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 PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: Bausch & Lomb Incorporated
NON-PROPRIETARY NAME: bepotastine besilate
SUBSTANCE NAME: BEPOTASTINE BESILATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Histamine-1 Receptor Antagonist [EPC]
ROUTE: OPHTHALMIC
DOSAGE FORM: SOLUTION/ DROPS
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2009-09-08
END MARKETING DATE: 0000-00-00


Bepreve HUMAN PRESCRIPTION DRUG Details:

Item DescriptionBepreve from Bausch & Lomb Incorporated
LABELER NAME: Bausch & Lomb Incorporated
DEA SCHEDULE:
ACTIVE STRENGTH: 15(mg/mL)
START MARKETING DATE: 2009-09-08
END MARKETING DATE: 0000-00-00
PRODUCT ID: 24208-629_edb50e66-e407-4d18-874a-4516802a30ed
PRODUCT NDC: 24208-629
APPLICATION NUMBER: NDA022288

Other BEPOTASTINE BESILATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Bausch & Lomb IncorporatedBepreve