Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 2Sanofi
02 4Taro Pharmaceutical Industries
03 1ALTANA
04 1APOTHEKERNES
05 1Antibiotice SA
06 8Bausch & Lomb Incorporated
07 1Bausch Health
08 3COMBE
09 2DELCOR ASSET
10 1Eli Lilly
11 1Exzell Pharma
12 1Flagship Biotech International Pvt. Ltd
13 1Fulton Medicinali S.p.A
14 1GSK
15 1JAMP PHARMA
16 6Johnson & Johnson
17 3NASKA
18 1ODAN LABORATORIES LTD
19 1PENDOPHARM DIVISION OF DE PHARMASCIENCE INC
20 4Padagis
21 1Perrigo Company plc
22 4Pfizer Inc
23 2Pharmaderm
24 2Pharmascience Inc.
25 2Quad Pharma
26 1STERI-MED PHARMA INC.
27 1STERIMAX INC
28 3ScieGen Pharmaceuticals
29 1TEOFARMA Srl
30 1Vega Biotech Pvt. Ltd.
31 2XGen Pharmaceuticals
32 1Xellia Pharmaceuticals ApS
33 1ZEE MEDICAL INC
01 1AEROSOL;TOPICAL
02 1Cream
03 1DISC;TOPICAL
04 2Injectable; Injection
05 1Injection
06 17OINTMENT
07 24OINTMENT;OPHTHALMIC
08 7OINTMENT;TOPICAL
09 1PDR
10 1POR
11 1POWDER FOR SOLUTION
12 4POWDER;FOR RX COMPOUNDING
13 1ointment
14 4Blank
01 29DISCN
02 1Ethical
03 3Generic
04 16OTC
05 2Originator
06 8RX
07 7Blank
01 1ANTIBIOTIC OINTMENT
02 1ANTIBIOTIC OINTMENT USP
03 1BACI-RX
04 1BACIGUENT
05 1BACIJECT
06 1BACIMYXIN ONGUENT
07 1BACITIN
08 10BACITRACIN
09 3BACITRACIN ZINC AND POLYMYXIN B SULFATE
10 2BACITRACIN ZINC-NEOMYCIN SULFATE-POLYMYXIN B SULFATE
11 1BACITRACIN ZINC-POLYMYXIN B SULFATE
12 1BACITRACIN-NEOMYCIN-POLYMYXIN
13 2BACITRACIN-NEOMYCIN-POLYMYXIN W/ HYDROCORTISONE ACETATE
14 1BAND-AID BRAND ADHESIVE BANDAGES PLUS ANTIBIOTIC
15 1BIODERM OINTMENT
16 2Bimixin
17 1COMPLETE ANTIBIOTIC OINTMENT
18 2CORTISPORIN
19 1Cicatrin Powder 15G
20 1Cicatrin Powder 15g
21 1Enterostop
22 1FIRST AID ANTIBIOTIC OINTMENT
23 1JAMPOLYCIN
24 2LANABIOTIC
25 1LUMI-SPORYN
26 1MYCITRACIN
27 1NEO-POLYCIN
28 1NEOMICINE/ZINC BACITRACINE
29 1NEOMYCIN & POLYMYXIN B SULFATES & BACITRACIN ZINC & HYDROCORTISONE
30 3NEOMYCIN AND POLYMYXIN B SULFATES AND BACITRACIN ZINC
31 2NEOMYCIN AND POLYMYXIN B SULFATES, BACITRACIN ZINC AND HYDROCORTISONE
32 1OCUMYCIN
33 1OZONOL ANTIBIOTICS PLUS
34 1Orobicin
35 1POLYDERM OINTMENT USP
36 2POLYSPORIN
37 1POLYSPORIN ANTIBIOTIC OINTMENT
38 1POLYSPORIN COMPLETE
39 1POLYSPORIN TRIPLE ANTIBIOTIC OINTMENT
40 1STERISPORIN
41 1TRIPLE ANTIBIOTIC OINTMENT
42 1Triple Antibiotic
43 1ZIBA-RX
44 1ZINC BACITRACIN,NEOMYCIN SULFATE,POLYMYXIN B SULFATE & HYDROCORTISONE
45 2Blank
01 17Canada
02 1Denmark
03 2India
04 4Italy
05 1Romania
06 2South Africa
07 39USA
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Italy
Brand Name : Bimixin
Dosage Form :
Dosage Strength : 16 Cpr 2,500 Iu + 25,000 Iu
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Italy
Brand Name : Bimixin
Dosage Form :
Dosage Strength : The Scir 60 Ml 15,000 Iu + 150,000 Iu
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info : OTC
Registration Country : Canada
Brand Name : POLYDERM OINTMENT USP
Dosage Form : OINTMENT
Dosage Strength : 500UNIT/G
Packaging : 15/30/450G
Approval Date :
Application Number : 2181908
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : OTC
Registration Country : Canada
Brand Name : ANTIBIOTIC OINTMENT USP
Dosage Form : OINTMENT
Dosage Strength : 500UNIT/G
Packaging : 15G
Approval Date :
Application Number : 2230251
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : OTC
Registration Country : Canada
Brand Name : TRIPLE ANTIBIOTIC OINTMENT
Dosage Form : OINTMENT
Dosage Strength : 500UNIT/G
Packaging : 15 G
Approval Date :
Application Number : 2246693
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : OTC
Registration Country : Canada
Brand Name : COMPLETE ANTIBIOTIC OINTMENT
Dosage Form : OINTMENT
Dosage Strength : 500UNIT/G
Packaging : 15G
Approval Date :
Application Number : 2304465
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : DISCN
Registration Country : USA
BACITRACIN; HYDROCORTISONE ACETATE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Brand Name : BACITRACIN-NEOMYCIN-POLYMYXIN W/ HYDROCORTISONE ACETATE
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : 400 UNITS/GM;1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM
Packaging :
Approval Date : 1982-01-01
Application Number : 60731
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
BACITRACIN ZINC; HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Brand Name : NEOMYCIN & POLYMYXIN B SULFATES & BACITRACIN ZINC & HYDROCORTISONE
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 400 UNITS/GM;1%;EQ 3.5MG BASE/GM;5,000 UNITS/GM
Packaging :
Approval Date : 1985-09-06
Application Number : 62381
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Brand Name : BACITRACIN ZINC-NEOMYCIN SULFATE-POLYMYXIN B SULFATE
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : 400 UNITS/GM;EQ 3.5MG BASE/GM;10,000 UNITS/GM
Packaging :
Approval Date : 1982-09-09
Application Number : 62386
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
BACITRACIN ZINC; HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Brand Name : ZINC BACITRACIN,NEOMYCIN SULFATE,POLYMYXIN B SULFATE & HYDROCORTISONE
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : 400 UNITS/GM;1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM
Packaging :
Approval Date : 1982-07-02
Application Number : 62389
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
BACITRACIN ZINC; POLYMYXIN B SULFATE
Brand Name : OCUMYCIN
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : 500 UNITS/GM;10,000 UNITS/GM
Packaging :
Approval Date : 1983-04-08
Application Number : 62430
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BACITRACIN
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : 500 UNITS/GM
Packaging :
Approval Date : 1984-03-28
Application Number : 62453
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Brand Name : NEO-POLYCIN
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : 500 UNITS/GM;EQ 3.5MG BASE/GM;10,000 UNITS/GM
Packaging :
Approval Date : 1982-01-01
Application Number : 60647
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Brand Name : LUMI-SPORYN
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : EQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM
Packaging :
Approval Date : 1982-01-01
Application Number : 50417
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BACITRACIN
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : 500 UNITS/GM
Packaging :
Approval Date : 1982-01-01
Application Number : 60687
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Brand Name : NEOMYCIN AND POLYMYXIN B SULFATES AND BACITRACIN ZINC
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 : 60764
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BACITRACIN
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : 500 UNITS/GM
Packaging :
Approval Date : 1982-01-01
Application Number : 61212
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
BACITRACIN ZINC; HYDROCORTISONE ACETATE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Brand Name : BACITRACIN-NEOMYCIN-POLYMYXIN W/ HYDROCORTISONE ACETATE
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : 400 UNITS/GM;1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM
Packaging :
Approval Date : 1982-01-01
Application Number : 62166
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BACIGUENT
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : 500 UNITS/GM
Packaging :
Approval Date : 1982-01-01
Application Number : 60734
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
BACITRACIN; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Brand Name : MYCITRACIN
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : 500 UNITS/GM;EQ 3.5MG BASE/GM;10,000 UNITS/GM
Packaging :
Approval Date : 1982-01-01
Application Number : 61048
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
BACITRACIN ZINC; POLYMYXIN B SULFATE
Brand Name : POLYSPORIN
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : 500 UNITS/GM;10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 61229
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BACITRACIN
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : 500 UNITS/GM
Packaging :
Approval Date : 1982-01-01
Application Number : 62158
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Brand Name : BACITRACIN-NEOMYCIN-POLYMYXIN
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : 400 UNITS/GM;EQ 3.5MG BASE/GM;5,000 UNITS/GM
Packaging :
Approval Date : 1982-01-01
Application Number : 62167
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BACI-RX
Dosage Form : POWDER;FOR RX COMPOUNDING
Dosage Strength : 5,000,000 UNITS/BOT
Packaging :
Approval Date : 1982-01-01
Application Number : 61580
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ZIBA-RX
Dosage Form : POWDER;FOR RX COMPOUNDING
Dosage Strength : 500,000 UNITS/BOT
Packaging :
Approval Date : 1982-01-01
Application Number : 61737
Regulatory Info : DISCN
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
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BACITRACIN
Dosage Form : POWDER;FOR RX COMPOUNDING
Dosage Strength : 5,000,000 UNITS/BOT
Packaging :
Approval Date : 1982-01-01
Application Number : 61699
Regulatory Info : DISCN
Registration Country : USA
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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