01 6Allergan Aesthetics
02 5Alcon Inc
03 13Bausch & Lomb Incorporated
04 5Bayer AG
05 1Chartwell Pharmaceuticals llc
06 6Epic Pharma. LLC.
07 2Farmak JSC
08 1Fougera Pharmaceuticals Inc.
09 1Genus Lifesciences
10 2MIZA PHARMS USA
11 4Novartis Pharmaceuticals Corporation
12 1OPTOPICS
13 2Padagis
14 2Pharmascience Inc.
15 1RENOVA PHARMS
16 4SOLA BARNES HIND
17 1Taro Pharmaceutical Industries
01 1DROPS
02 2Eye Drop
03 1LIQUID
04 4LOTION;TOPICAL
05 10OINTMENT;OPHTHALMIC
06 31SOLUTION/DROPS;OPHTHALMIC
07 6SUSPENSION/DROPS;OPHTHALMIC
08 2SUSPENSION;OPHTHALMIC
01 45DISCN
02 2Prescription
03 8RX
04 2Blank
01 2BLEPH-10
02 1BLEPH-30
03 1BLEPHAMIDE
04 1BLEPHAMIDE S.O.P.
05 1CETAMIDE
06 1CETAPRED
07 1FML-S
08 1ISOPTO CETAMIDE
09 1ISOPTO CETAPRED
10 1KLARON
11 2METIMYD
12 1OCUSULF-10
13 1OCUSULF-30
14 1PMS-SULFACETAMIDE SOD OPH SOLN 30%
15 1PMS-SULFACETAMIDE SODIUM LIQ 10%
16 1PREDAMIDE
17 2PREDSULFAIR
18 1PREDSULFAIR II
19 3SODIUM SULAMYD
20 7SODIUM SULFACETAMIDE
21 1SULF-10
22 1SULF-15
23 1SULFACEL-15
24 10SULFACETAMIDE SODIUM
25 2SULFACETAMIDE SODIUM AND PREDNISOLONE SODIUM PHOSPHATE
26 2SULFAIR 10
27 1SULFAIR FORTE
28 1SULFAIR-15
29 1SULPHRIN
30 1SULSTER
31 1SULTEN-10
32 2Sulfacil
33 2VASOCIDIN
01 2Canada
02 53USA
03 2Ukraine
Regulatory Info : DISCN
Registration Country : USA
PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM
Brand Name : BLEPHAMIDE
Dosage Form : SUSPENSION;OPHTHALMIC
Dosage Strength : 0.2%;10%
Packaging :
Approval Date : 1982-01-01
Application Number : 12813
Regulatory Info : DISCN
Registration Country : USA
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 : DISCN
Registration Country : USA
Brand Name : BLEPH-10
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 10%
Packaging :
Approval Date : 1982-01-01
Application Number : 80028
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BLEPH-30
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 30%
Packaging :
Approval Date : 1982-01-01
Application Number : 80028
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BLEPH-10
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : 10%
Packaging :
Approval Date : 1982-01-01
Application Number : 84015
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM
Brand Name : BLEPHAMIDE S.O.P.
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : 0.2%;10%
Packaging :
Approval Date : 1986-12-03
Application Number : 87748
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : KLARON
Dosage Form : LOTION;TOPICAL
Dosage Strength : 10%
Packaging :
Approval Date : 1996-12-23
Application Number : 19931
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : SULFACETAMIDE SODIUM
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 10%
Packaging :
Approval Date : 1994-12-28
Application Number : 40066
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
PREDNISOLONE SODIUM PHOSPHATE; SULFACETAMIDE SODIUM
Brand Name : SULFACETAMIDE SODIUM AND PREDNISOLONE SODIUM PHOSPHATE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.23% PHOSPHATE;10%
Packaging :
Approval Date : 1995-12-29
Application Number : 74449
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SODIUM SULAMYD
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 10% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 5963
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SODIUM SULAMYD
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : 10% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 5963
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SODIUM SULAMYD
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 30% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 5963
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM
Brand Name : METIMYD
Dosage Form : SUSPENSION/DROPS;OPHTHALMIC
Dosage Strength : 0.5%;10%
Packaging :
Approval Date : 1982-01-01
Application Number : 10210
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM
Brand Name : METIMYD
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : 0.5%;10%
Packaging :
Approval Date : 1984-09-09
Application Number : 10210
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SULFACETAMIDE SODIUM
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 30%
Packaging :
Approval Date : 1999-05-25
Application Number : 40216
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
PREDNISOLONE SODIUM PHOSPHATE; SULFACETAMIDE SODIUM
Brand Name : SULSTER
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.23% PHOSPHATE;10%
Packaging :
Approval Date : 1996-07-30
Application Number : 74511
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : SULFACETAMIDE SODIUM
Dosage Form : LOTION;TOPICAL
Dosage Strength : 10%
Packaging :
Approval Date : 2006-11-17
Application Number : 77015
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
PREDNISOLONE SODIUM PHOSPHATE; SULFACETAMIDE SODIUM
Brand Name : SULFACETAMIDE SODIUM AND PREDNISOLONE SODIUM PHOSPHATE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.23% PHOSPHATE;10%
Packaging :
Approval Date : 1993-05-27
Application Number : 73630
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
PREDNISOLONE SODIUM PHOSPHATE; SULFACETAMIDE SODIUM
Brand Name : VASOCIDIN
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.23% PHOSPHATE;10% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1988-08-26
Application Number : 18988
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SULFACETAMIDE SODIUM
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 10%
Packaging :
Approval Date : 1999-05-25
Application Number : 40215
Regulatory Info : DISCN
Registration Country : USA
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