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01 7AbbVie Inc
02 2Allergan Aesthetics
03 1Adcock Ingram
04 1Alcon Inc
05 1Amneal Pharmaceuticals
06 1Arafarma
07 5FARMILA-THEA FARMACEUTICI SpA
08 5Hanlim Pharmaceuticals Inc
09 1Immedica Pharma
10 1Indiana Ophthalmics
11 1Kolmar Korea Co., Ltd.
12 1Novartis Pharmaceuticals Corporation
13 1Novartis South Africa (Pty) Ltd
14 1Pfizer Inc
15 1Pharmascience Inc.
16 1Sandoz B2B
17 3TUBILUX PHARMA SpA
18 2Unimed Pharm Inc.
19 2Winston Medical Supply
20 4World Medicine
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01 1CREAM;TOPICAL
02 1Cream
03 4EYE DROP
04 4EYE DROPS
05 1EYE OINTMENT
06 1Eye Drop
07 4Eye Drop Suspension
08 1Eye Drops
09 2Eye Suspension
10 1OINTMENT;OPHTHALMIC
11 3OPD
12 2OPTHALMIC SOLUTION
13 3SUSPENSION
14 5SUSPENSION/DROPS;OPHTHALMIC
15 9Blank
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01 2Allowed
02 2Authorized
03 1Cancelled
04 4DISCN
05 9Generic
06 3Originator
07 3Prescription
08 3RX
09 15Blank
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01 2DIGENTA
02 1Efemoline
03 1FLOROLIFE
04 1FLUOR-OP
05 1FLUOROMETHOLONE
06 3FML
07 1FML FORTE
08 1FML Liquifilm
09 1FML Liquifilm Sterile Eye Suspension
10 1FML-Neo Liquifilm
11 1FML-S
12 1FORMIZOR
13 2FUMELON
14 1FUMELON-PLUS
15 1Flarex
16 1Flu Eyen Drops
17 2Fluaton
18 1Fluaton Pva
19 1Flucon
20 1Flumeciclina
21 3Flumetol
22 1Flumezina
23 1Fml
24 2Haoshiduo
25 1Isopto Flucon
26 1OXYLONE
27 1PMS-FLUOROMETHOLONE
28 1SANDOZ FLUOROMETHOLONE
29 1Solubalm
30 1Unimed Fluorometholone
31 1Unimelone
32 3Blank
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01 3Canada
02 1India
03 9Italy
04 3South Africa
05 8South Korea
06 3Spain
07 2Switzerland
08 2Taiwan
09 4Turkey
10 7USA
Regulatory Info : RX
Registration Country : USA
Brand Name : FML
Dosage Form : SUSPENSION/DROPS;OPHTHALMIC
Dosage Strength : 0.1%
Packaging :
Approval Date : 1982-07-28
Application Number : 16851
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FML
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : 0.1%
Packaging :
Approval Date : 1985-09-04
Application Number : 17760
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : FML FORTE
Dosage Form : SUSPENSION/DROPS;OPHTHALMIC
Dosage Strength : 0.25%
Packaging :
Approval Date : 1986-04-23
Application Number : 19216
Regulatory Info : RX
Registration Country : USA
Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : FML Liquifilm
Dosage Form : Eye Drop Suspension
Dosage Strength : 1mg/ml
Packaging :
Approval Date : 17/10/1973
Application Number : 38084
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : FML-Neo Liquifilm
Dosage Form : Eye Drop Suspension
Dosage Strength :
Packaging :
Approval Date : 01/04/1974
Application Number : 38174
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : FML
Dosage Form : SUSPENSION
Dosage Strength : 0.1%/W/V
Packaging :
Approval Date :
Application Number : 247855
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : FML Liquifilm Sterile Eye Suspension
Dosage Form : OPD
Dosage Strength : 1mg/ml
Packaging : 5X1mg/ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Fml
Dosage Form : Eye Drop Suspension
Dosage Strength : 1MG
Packaging :
Approval Date : 1988-03-01
Application Number : 57606
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : DISCN
Registration Country : USA
FLUOROMETHOLONE; SULFACETAMIDE SODIUM
Brand Name : FML-S
Dosage Form : SUSPENSION/DROPS;OPHTHALMIC
Dosage Strength : 0.1%;10%
Packaging :
Approval Date : 1989-09-29
Application Number : 19525
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : FLUOROMETHOLONE
Dosage Form : SUSPENSION/DROPS;OPHTHALMIC
Dosage Strength : 0.1%
Packaging :
Approval Date : 2024-01-09
Application Number : 216348
Regulatory Info : RX
Registration Country : USA
Regulatory Info : Generic
Registration Country : South Korea
GENTAMICIN SULFATE; Fluorometholone
Brand Name : DIGENTA
Dosage Form : EYE DROP
Dosage Strength : 3MG/ML; 1MG/ML
Packaging : 5mL
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Korea
Regulatory Info : Generic
Registration Country : South Korea
Brand Name : FUMELON
Dosage Form : EYE DROP
Dosage Strength : 1MG/ML
Packaging : 5mL & 0.6mL*30ea
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Korea
Regulatory Info : Generic
Registration Country : South Korea
Brand Name : FUMELON
Dosage Form : EYE DROP
Dosage Strength : 0.2MG/ML
Packaging : 5mL
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Korea
Regulatory Info : Generic
Registration Country : South Korea
Brand Name : FUMELON-PLUS
Dosage Form : EYE DROP
Dosage Strength : 1;0.25MG;MG/ML;ML
Packaging : 5mL
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Korea
Regulatory Info : Generic
Registration Country : South Korea
GENTAMICIN SULFATE; Fluorometholone
Brand Name : DIGENTA
Dosage Form : EYE OINTMENT
Dosage Strength : 3MG/G; 1MG/G
Packaging : 4g
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Korea
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FLUOR-OP
Dosage Form : SUSPENSION/DROPS;OPHTHALMIC
Dosage Strength : 0.1%
Packaging :
Approval Date : 1986-02-27
Application Number : 70185
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : OXYLONE
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.025%
Packaging :
Approval Date : 1982-01-01
Application Number : 11748
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : Generic
Registration Country : South Korea
Brand Name : Unimed Fluorometholone
Dosage Form : OPTHALMIC SOLUTION
Dosage Strength : 1MG
Packaging : Blow Fill Seal System (BFS)
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Korea
Regulatory Info : Generic
Registration Country : South Korea
Fluorometholone; Tetrahydrozoline
Brand Name : Unimelone
Dosage Form : OPTHALMIC SOLUTION
Dosage Strength : 1MG; 0.25MG
Packaging : Blow Fill Seal System (BFS)
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Korea
Regulatory Info : Generic
Registration Country : Turkey
Brand Name :
Dosage Form : EYE DROPS
Dosage Strength : 0.1%
Packaging : 5 Ml/Bottle
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : Turkey