FML - 11980-211-10 - (fluorometholone)

Alphabetical Index


Drug Information of FML

Product NDC: 11980-211
Proprietary Name: FML
Non Proprietary Name: fluorometholone
Active Ingredient(s): 1    mg/mL & nbsp;   fluorometholone
Administration Route(s): OPHTHALMIC
Dosage Form(s): SUSPENSION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of FML

Product NDC: 11980-211
Labeler Name: Allergan, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA016851
Marketing Category: NDA
Start Marketing Date: 19720201

Package Information of FML

Package NDC: 11980-211-10
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (11980-211-10) > 10 mL in 1 BOTTLE, DROPPER

NDC Information of FML

NDC Code 11980-211-10
Proprietary Name FML
Package Description 1 BOTTLE, DROPPER in 1 CARTON (11980-211-10) > 10 mL in 1 BOTTLE, DROPPER
Product NDC 11980-211
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fluorometholone
Dosage Form Name SUSPENSION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 19720201
Marketing Category Name NDA
Labeler Name Allergan, Inc.
Substance Name FLUOROMETHOLONE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of FML


General Information