FML FORTE (Allergan, Inc.)


Welcome to the PulseAid listing for the FML FORTE drug offered from Allergan, Inc.. 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: Allergan, Inc.
NON-PROPRIETARY NAME: fluorometholone
SUBSTANCE NAME: FLUOROMETHOLONE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
ROUTE: OPHTHALMIC
DOSAGE FORM: SUSPENSION/ DROPS
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 1986-05-01
END MARKETING DATE: 0000-00-00


FML FORTE HUMAN PRESCRIPTION DRUG Details:

Item DescriptionFML FORTE from Allergan, Inc.
LABELER NAME: Allergan, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 2.5(mg/mL)
START MARKETING DATE: 1986-05-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 11980-228_86169620-8649-4b2d-aa5f-b7ab057f489b
PRODUCT NDC: 11980-228
APPLICATION NUMBER: NDA019216

Other FLUOROMETHOLONE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Allergan, Inc.FML
Pacific Pharma, Inc.FLUOROMETHOLONE