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

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01 1 Ophthalmic Suspension Drops
02 1AEROSOL;TOPICAL
03 3CREAM
04 2CREAM;TOPICAL
05 1Cream
06 1DISC;TOPICAL
07 1DROPS
08 1EAR
09 2EYE AND EAR DROPS
10 1EYE OINTMENT
11 1EYO
12 2Ear Drop
13 1Ear Drop Solution
14 2Ear Drops
15 5Eye Drop
16 2Eye Drops
17 1Eye Drops Suspension
18 1Eye Ointment
19 1Eye Suspension
20 11Eye/Ear Drops
21 4Eye/Ear Ointment
22 8INJECTABLE;INJECTION
23 4Injection
24 1LIQUID
25 2Lyo.Inj
26 1Lyophilised Injection
27 1Lyophilized Injection
28 2NASAL SPRAY
29 1Nasal Spray Solution
30 3OIN
31 9OINTMENT
32 28OINTMENT;OPHTHALMIC
33 1OINTMENT;OTIC
34 5OINTMENT;TOPICAL
35 1OPD
36 2Ointment
37 1Ophthalmic Ointment
38 2Ophthalmic Solution
39 2POWDER;FOR RX COMPOUNDING
40 1PVC
41 2SOLUTION
42 14SOLUTION/DROPS;OPHTHALMIC
43 9SOLUTION/DROPS;OTIC
44 1SOLUTION; IRRIGATION
45 4SOLUTION;IRRIGATION
46 1SUS
47 4SUSPENSION
48 10SUSPENSION/DROPS;OPHTHALMIC
49 10SUSPENSION/DROPS;OTIC
50 1Salve
51 2Soft Capsule
52 2Suspension For Injection
53 1TABLET;VAGINAL
54 1Tablet
55 1Unguent Oftalmic
56 1Vial
57 1Blank
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02 6Approved
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04 7Authorized
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06 59DISCN
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08 12Generic
09 9NON-PRESCRIPTION DRUGS
10 2OTC
11 6Originator
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13 37RX
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15 17Blank
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01 1AEROSPORIN
02 1ANTIBIOTIC CREAM FOR KIDS
03 1ANTIBIOTIC OINTMENT
04 1ANTIBIOTIC OINTMENT USP
05 1ANTIBIOTIC PLUS PAIN RELIEF CREAM
06 1AURIMIC
07 1Adacel-Polio
08 1Anauran®
09 1Antibiotic Cream
10 1BACIMYXIN ONGUENT
11 3BACITRACIN ZINC AND POLYMYXIN B SULFATE
12 2BACITRACIN ZINC-NEOMYCIN SULFATE-POLYMYXIN B SULFATE
13 1BACITRACIN ZINC-POLYMYXIN B SULFATE
14 1BACITRACIN-NEOMYCIN-POLYMYXIN
15 2BACITRACIN-NEOMYCIN-POLYMYXIN W/ HYDROCORTISONE ACETATE
16 1BAND-AID BRAND ADHESIVE BANDAGES PLUS ANTIBIOTIC
17 1Boostrix Polio
18 1CASPORYN HC
19 1CHLOROMYXIN
20 1COMPLETE ANTIBIOTIC OINTMENT
21 5CORTISPORIN
22 2DEXACIDIN
23 3DEXASPORIN
24 1Isopto-Biotic
25 2LANABIOTIC
26 1LUMI-SPORYN
27 1Liade Antibiotic Ointment
28 5MAXITROL
29 1MYCITRACIN
30 4Maxitrol
31 1Maxitrol Eye Drops
32 1Maxitrol Ointment
33 2Maxitrol®
34 1Mixotone
35 1NELADEX
36 1NELADEX-NS
37 2NEO-POLYCIN
38 1NEODEX
39 1NEOMYCIN & POLYMYXIN B SULFATES & BACITRACIN ZINC & HYDROCORTISONE
40 3NEOMYCIN AND POLYMYXIN B SULFATE
41 3NEOMYCIN AND POLYMYXIN B SULFATES AND BACITRACIN ZINC
42 3NEOMYCIN AND POLYMYXIN B SULFATES AND DEXAMETHASONE
43 4NEOMYCIN AND POLYMYXIN B SULFATES AND GRAMICIDIN
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45 2NEOMYCIN AND POLYMYXIN B SULFATES, BACITRACIN ZINC AND HYDROCORTISONE
46 1NEOMYCIN SULFATE AND POLYMYXIN B SULFATE GRAMICIDIN
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49 2NEOSPORIN
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51 1Nasal Synalar
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65 1PEDIOTIC
66 1PMS-POLYTRIMETHOPRIM
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70 1POLYGYNAX®
71 8POLYMYXIN B SULFATE
72 2POLYSPORIN
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74 1POLYTRIM
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77 1Paroticin (1 +
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84 3STATROL
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88 1TERRAMYCIN W/ POLYMYXIN
89 1TERRAMYCIN W/ POLYMYXIN B SULFATE
90 1TERRAMYCIN-POLYMYXIN
91 4TRIMETHOPRIM SULFATE AND POLYMYXIN B SULFATE
92 3Terra-Cortril With Polymyxin B
93 1Terracortril
94 1Terracortril Sterile Otic-Ophthalmic Ointment
95 12Terracortril With Polymyxin B
96 1Terramycin Topical Ointment
97 1Terramycin topical ointment
98 1Terramycin-Polymyxin B
99 1Triple Antibiotic
100 1Videtrol
101 1Vinciseptil Ear Drops In Solution
102 1ZINC BACITRACIN,NEOMYCIN SULFATE,POLYMYXIN B SULFATE & HYDROCORTISONE
103 12Blank
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01 20Canada
02 1Denmark
03 1Egypt
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06 2Malta
07 4Moldova
08 8South Africa
09 3South Korea
10 10Spain
11 17Sweden
12 6Switzerland
13 4Turkey
14 1U.S.A
15 97USA
16 1Vietnam
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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