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Fluor-opDrug - Fluor-op The trade name of the product as shown on the labeling.
Dosage -
SUSPENSION; OPHTHALMIC
Active Ingredient(s) -
Fluorometholone
Strength -
0.1%
Applicant -
NOVARTIS
New Drug Application (NDA) Number -
070185
Product Number -
001
Therapeutic Equivalence (TE) Code -
AB
Approval Date -
Feb 27, 1986
Reference Listed Drug (RLD) -
No
Type -
RX
Applicant Full Name -
Novartis Pharmaceuticals Corp
Fluor-op
Lidex 0.05% Solution; Topical
Funduscein-25 25% Injectable; Injection Oxylone 0.025% Cream; Topical Fml 0.1% Ointment; Ophthalmic Fml 0.1% Suspension/drops; Ophthalmic Fml Forte 0.25% Suspension/drops; Ophthalmic Fluor-op 0.1% Suspension; Ophthalmic Fluocinonide 0.05% Solution; Topical Fluocinonide 0.05% Solution; Topical Fluocinonide 0.05% Solution; Topical NewDrugInformation |