Flunisolide (Bausch & Lomb Incorporated)


Welcome to the PulseAid listing for the Flunisolide drug offered from Bausch & Lomb Incorporated. This Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] 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: Flunisolide
SUBSTANCE NAME: FLUNISOLIDE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
ROUTE: NASAL
DOSAGE FORM: SOLUTION
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 2002-02-20
END MARKETING DATE: 0000-00-00


Flunisolide HUMAN PRESCRIPTION DRUG Details:

Item DescriptionFlunisolide from Bausch & Lomb Incorporated
LABELER NAME: Bausch & Lomb Incorporated
DEA SCHEDULE:
ACTIVE STRENGTH: 0.25(mg/mL)
START MARKETING DATE: 2002-02-20
END MARKETING DATE: 0000-00-00
PRODUCT ID: 24208-344_69e7e721-ce22-442c-ac61-e9ca802477a1
PRODUCT NDC: 24208-344
APPLICATION NUMBER: ANDA074805

Other FLUNISOLIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Acton Pharmaceuticals, Inc.Aerospan
Bausch & Lomb IncorporatedFlunisolide
Meda PharmaceuticalsAerospan
Physicians Total Care, Inc.Flunisolide
REMEDYREPACK INC.Flunisolide
Rising Pharmaceuticals, IncFlunisolide