Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

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Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Allowed
Registration Country : Switzerland
Diphtheria Toxoid; Tetanus Toxoid; Bordetella Pertussis Antigen; Inactivated Poliovirus Types 1, 2, 3; Diphtheria Toxoid; Tetanus Toxoid; Bordetella Pertussis Antigen; Inactivated Poliovirus Types 1, 2, 3; Polymyxin B; Haemophilus Influenzae Type B Polysaccharide Conjugated With Tetanus Toxoid; Pertussis Fimbriae
Brand Name : Adacel-Polio
Dosage Form : Suspension For Injection
Dosage Strength :
Packaging :
Approval Date : 26/08/2022
Application Number : 68110
Regulatory Info : Allowed
Registration Country : Switzerland
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Regulatory Info : DISCN
Registration Country : USA
NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PREDNISOLONE ACETATE
Brand Name : POLY-PRED
Dosage Form : SUSPENSION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.35% BASE;10,000 UNITS/ML;0.5%
Packaging :
Approval Date : 1982-01-01
Application Number : 50081
Regulatory Info : DISCN
Registration Country : USA
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Regulatory Info : DISCN
Registration Country : USA
POLYMYXIN B SULFATE; TRIMETHOPRIM SULFATE
Brand Name : POLYTRIM
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 10,000 UNITS/ML;EQ 1MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1988-10-20
Application Number : 50567
Regulatory Info : DISCN
Registration Country : USA
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Regulatory Info : DISCN
Registration Country : USA
NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Brand Name : STATROL
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : EQ 3.5MG BASE/GM;10,000 UNITS/GM
Packaging :
Approval Date : 1982-01-01
Application Number : 50344
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Brand Name : STATROL
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 3.5MG BASE/ML;16,250 UNITS/ML
Packaging :
Approval Date : 1982-01-01
Application Number : 50456
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
GRAMICIDIN; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Brand Name : NEO-POLYCIN
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 0.025MG/ML;EQ 1.75MG BASE/ML;10,000 UNITS/ML
Packaging :
Approval Date : 1982-01-01
Application Number : 60427
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
BACITRACIN ZINC; HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Brand Name : CORTISPORIN
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : 400 UNITS/GM;1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 50416
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Brand Name : LUMI-SPORYN
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : 400 UNITS/GM;EQ 3.5MG BASE/GM;10,000 UNITS/GM
Packaging :
Approval Date : 1982-01-01
Application Number : 50417
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
BACITRACIN ZINC; POLYMYXIN B SULFATE
Brand Name : POLYSPORIN
Dosage Form : AEROSOL;TOPICAL
Dosage Strength : 10,000 UNITS/GM;2,000,000 UNITS/GM
Packaging :
Approval Date : 1985-03-01
Application Number : 50167
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Brand Name : NEOSPORIN
Dosage Form : CREAM;TOPICAL
Dosage Strength : EQ 3.5MG BASE/GM;10,000 UNITS/GM
Packaging :
Approval Date : 1985-01-14
Application Number : 50176
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
DEXAMETHASONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Brand Name : MAXITROL
Dosage Form : SUSPENSION/DROPS;OPHTHALMIC
Dosage Strength : 0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML
Packaging :
Approval Date : 1982-01-01
Application Number : 50023
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
BACITRACIN ZINC; HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Brand Name : CORTISPORIN
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 400 UNITS/GM;1%;EQ 3.5MG BASE/GM;5,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1984-05-04
Application Number : 50168
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Brand Name : CORTISPORIN
Dosage Form : SUSPENSION/DROPS;OPHTHALMIC
Dosage Strength : 1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML
Packaging :
Approval Date : 1982-01-01
Application Number : 50169
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
CHLORAMPHENICOL; HYDROCORTISONE ACETATE; POLYMYXIN B SULFATE
Brand Name : OPHTHOCORT
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : 10MG/GM;5MG/GM;10,000 UNITS/GM
Packaging :
Approval Date : 1982-01-01
Application Number : 50201
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
CHLORAMPHENICOL; POLYMYXIN B SULFATE
Brand Name : CHLOROMYXIN
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : 1%;10,000 UNITS/GM
Packaging :
Approval Date : 1982-01-01
Application Number : 50203
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
HYDROCORTISONE ACETATE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Brand Name : CORTISPORIN
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.5%;EQ 3.5MG BASE/GM;10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1985-08-09
Application Number : 50218
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Brand Name : CORTISPORIN
Dosage Form : SOLUTION/DROPS;OTIC
Dosage Strength : 1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 50479
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
GRAMICIDIN; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Brand Name : NEOSPORIN
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 0.025MG/ML;EQ 1.75MG BASE/ML;10,000 UNITS/ML
Packaging :
Approval Date : 1982-01-01
Application Number : 60582
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
DEXAMETHASONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Brand Name : MAXITROL
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : 0.1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM
Packaging :
Approval Date : 1982-01-01
Application Number : 50065
Regulatory Info : RX
Registration Country : USA

Regulatory Info : DISCN
Registration Country : USA
BACITRACIN; POLYMYXIN B SULFATE
Brand Name : LANABIOTIC
Dosage Form : DISC;TOPICAL
Dosage Strength : 500 UNITS/GM;5,000 UNITS/GM
Packaging :
Approval Date : 1986-09-22
Application Number : 50598
Regulatory Info : DISCN
Registration Country : USA

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