FML (Allergan, Inc.)


Welcome to the PulseAid listing for the FML 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: OINTMENT
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 1985-12-09
END MARKETING DATE: 0000-00-00


FML HUMAN PRESCRIPTION DRUG Details:

Item DescriptionFML from Allergan, Inc.
LABELER NAME: Allergan, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 1(mg/g)
START MARKETING DATE: 1985-12-09
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0023-0316_9c77b0ad-2660-4ef1-bd0c-c98c80310633
PRODUCT NDC: 0023-0316
APPLICATION NUMBER: NDA017760

Other FLUOROMETHOLONE Pharmaceutical Manufacturers / Labelers:

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