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01 2APRACLONIDINE HYDROCHLORIDE
02 1CETIRIZINE HYDROCHLORIDE
03 1CHLOROPROCAINE HYDROCHLORIDE
04 1CLOBETASOL PROPIONATE
05 2CYCLOSPORINE
06 1DEXAMETHASONE
07 1DEXAMETHASONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
08 1DEXAMETHASONE; TOBRAMYCIN
09 1FLUOROMETHOLONE ACETATE
10 1FLUOROMETHOLONE ACETATE; TOBRAMYCIN
11 2MOXIFLOXACIN HYDROCHLORIDE
12 1NATAMYCIN
13 2NEPAFENAC
14 1PREDNISOLONE ACETATE
15 1RIMEXOLONE
16 1TRIAMCINOLONE ACETONIDE
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01 1EMULSION;OPHTHALMIC
02 1GEL;OPHTHALMIC
03 1INJECTABLE;INTRAVITREAL
04 5SOLUTION/DROPS;OPHTHALMIC
05 1SOLUTION;OPHTHALMIC
06 10SUSPENSION/DROPS;OPHTHALMIC
07 1SUSPENSION;OPHTHALMIC
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01 10.05%
02 10.05%;0.3%
03 50.1%
04 10.1%;0.3%
05 10.1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML
06 10.125%
07 10.3%
08 11%
09 13%
10 140MG/ML (40MG/ML)
11 15%
12 1EQ 0.24% BASE
13 2EQ 0.5% BASE
14 1EQ 0.5% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
15 1EQ 1% BASE
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01 4DISCN
02 16RX
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RLD : Yes
TE Code :
Dosage Form : SOLUTION/DROPS; OPHTHALMIC
Proprietary Name : IOPIDINE
Dosage Strength : EQ 1% BASE
Approval Date : 1987-12-31
Application Number : 19779
RX/OTC/DISCN : RX
RLD : Yes
TE Code :

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RLD : Yes
TE Code : AT
Dosage Form : SOLUTION/DROPS; OPHTHALMIC
Proprietary Name : IOPIDINE
Dosage Strength : EQ 0.5% BASE
Approval Date : 1993-07-30
Application Number : 20258
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AT

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RLD : Yes
TE Code :
Dosage Form : SOLUTION/DROPS; OPHTHALMIC
Proprietary Name : ZERVIATE
Dosage Strength : EQ 0.24% BASE
Approval Date : 2017-05-30
Application Number : 208694
RX/OTC/DISCN : RX
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
Dosage Form : GEL; OPHTHALMIC
Proprietary Name : IHEEZO
Dosage Strength : 3%
Approval Date : 2022-09-27
Application Number : 216227
RX/OTC/DISCN : RX
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
Dosage Form : SUSPENSION/DROPS; OPHTHALMIC
Proprietary Name : BYQLOVI
Dosage Strength : 0.05%
Approval Date : 2024-03-04
Application Number : 218158
RX/OTC/DISCN : RX
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
Dosage Form : EMULSION; OPHTHALMIC
Proprietary Name : VERKAZIA
Dosage Strength : 0.1%
Approval Date : 2021-06-23
Application Number : 214965
RX/OTC/DISCN : RX
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
Dosage Form : SOLUTION; OPHTHALMIC
Proprietary Name : VEVYE
Dosage Strength : 0.1%
Approval Date : 2023-05-30
Application Number : 217469
RX/OTC/DISCN : RX
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
Dosage Form : SUSPENSION/DROPS; OPHTHALMIC
Proprietary Name : MAXIDEX
Dosage Strength : 0.1%
Approval Date : 1982-01-01
Application Number : 13422
RX/OTC/DISCN : RX
RLD : Yes
TE Code :

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RLD : Yes
TE Code : AT
DEXAMETHASONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Dosage Form : SUSPENSION/DROPS; OPHTHALMIC
Proprietary Name : MAXITROL
Dosage Strength : 0.1%;EQ 3.5MG BASE/ML;10...
Approval Date : 1982-01-01
Application Number : 50023
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AT

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RLD : Yes
TE Code :
Dosage Form : SUSPENSION/DROPS; OPHTHALMIC
Proprietary Name : TOBRADEX ST
Dosage Strength : 0.05%;0.3%
Approval Date : 2009-02-13
Application Number : 50818
RX/OTC/DISCN : RX
RLD : Yes
TE Code :

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