01 1AbbVie Inc
02 1Allergan Aesthetics
03 1Polfa Tarchomin
04 1ADRASTEA PHARMA
05 1ALFA INTES (IND.TER.SPLENDORE)
06 1ALTANA
07 4Actavis Inc
08 5Alcon Inc
09 2Amring Pharma
10 2Antibiotice SA
11 2BIO AGRI MIX LP
12 19Bausch & Lomb Incorporated
13 2Bausch Health
14 4Bayer AG
15 1Belfar
16 2Bharat Parenterals Limited
17 2Biodeal Pharmaceuticals
18 1Bristol Myers Squibb
19 2CAN-VET ANIMAL HEALTH SUPPLIES
20 1COMBE
21 1Chartwell Pharmaceuticals llc
22 3DELCOR ASSET
23 1DOMINION VETERINARY LABORATORIES LTD.
24 5Dong Bang Co., Ltd
25 1ENDO OPERATIONS
26 3Eli Lilly
27 1Epic Pharma. LLC.
28 2Flagship Biotech International Pvt. Ltd
29 2Fougera Pharmaceuticals Inc.
30 2GSK
31 1Glenmark Pharmaceuticals
32 1Hanlim Pharmaceuticals Inc
33 1Harrow
34 2Kolmar Korea Co., Ltd.
35 1Lannett Company, Inc.
36 1MEDIMETRIKS PHARMS
37 2Meracine
38 3Merck & Co
39 1Modern Laboratories
40 1NASKA
41 1Nordic Pharma
42 1Nostrum Laboratories
43 2Novartis Pharmaceuticals Corporation
44 1PHIBRO ANIMAL HEALTH CORPORATION
45 1PVS Laboratories
46 3Padagis
47 27Pfizer Inc
48 1Pharmacorp (Pty) Ltd
49 3Pharmaderm
50 2Qilu Animal Health Products
51 1ROXANE
52 6Sandoz B2B
53 2Savage Lab
54 2ScieGen Pharmaceuticals
55 1Seoul Pharma Co Ltd
56 1Shijiazhuang Fengqiang Animal Pharmaceutical Co., Ltd
57 2TEOFARMA Srl
58 1Teva Pharmaceutical Industries
59 1VETOQUINOL N A INC
60 2World Medicine
61 4XGen Pharmaceuticals
62 2Xepa-Soul Pattinson m SDN BHD
63 1ZRS LABS
64 1iPharma
01 1CRE
02 1CREAM
03 13CREAM;TOPICAL
04 9Cream
05 1DRUG PREMIX
06 1EAR
07 2EYE AND EAR DROPS
08 1EYE OINTMENT
09 1EYE/ EAR DROPS
10 1Eye Drop
11 1Eye Drops Suspension
12 2OINTMENT
13 27OINTMENT;OPHTHALMIC
14 11OINTMENT;TOPICAL
15 1OPD
16 4POWDER FOR SOLUTION
17 1POWDER;FOR RX COMPOUNDING
18 1PVC
19 3Powder
20 2Premix
21 13SOLUTION/DROPS;OPHTHALMIC
22 6SOLUTION/DROPS;OTIC
23 1SOLUTION; IRRIGATION
24 4SOLUTION;IRRIGATION
25 2SOLUTION;ORAL
26 1SUSPENSION
27 14SUSPENSION/DROPS;OPHTHALMIC
28 11SUSPENSION/DROPS;OTIC
29 1Soft Capsule
30 3Soluble Powder
31 1Suspension for Cutaneous Spray
32 11TABLET;ORAL
33 1Topical Cream
34 1WSP / Premix
35 1cream
36 1ointment
37 3Blank
01 83DISCN
02 1Dossier Available
03 9Generic
04 2Originator
05 7Prescription
06 29RX
07 28Blank
01 1Antibiotic Cream
02 2BACITRACIN ZINC-NEOMYCIN SULFATE-POLYMYXIN B SULFATE
03 1BACITRACIN-NEOMYCIN-POLYMYXIN
04 2BACITRACIN-NEOMYCIN-POLYMYXIN W/ HYDROCORTISONE ACETATE
05 1Betacortazol
06 1CASPORYN HC
07 1COLY-MYCIN S
08 1COR-OTICIN
09 2CORDRAN N
10 5CORTISPORIN
11 1COZIDERM
12 2DEXACIDIN
13 3DEXASPORIN
14 1Dermclear
15 1Desalfa
16 1Dextracin
17 1FLUOCINOLONE N Atb®
18 1FML Neo Liquifilm Ophthalmic Suspension
19 1Halciderm Combi
20 1KESERASIN
21 1LANABIOTIC
22 1LUMI-SPORYN
23 3MAXITROL
24 2MYCIFRADIN
25 1MYCITRACIN
26 2MYTREX A
27 1Mixotone
28 1NELADEX
29 1NEO-CHLOR
30 3NEO-CORT-DOME
31 9NEO-CORTEF
32 3NEO-DELTA-CORTEF
33 1NEO-FRADIN
34 1NEO-HYDELTRASOL
35 1NEO-MEDROL
36 2NEO-MEDROL ACETATE
37 2NEO-POLYCIN
38 1NEO-RX
39 1NEO-SYNALAR
40 1NEO-TERRAMYCIN 50/50
41 1NEO-TETRAMED
42 1NEO-TETRAPRO
43 1NEOBIOTIC
44 2NEODECADRON
45 1NEODEX
46 1NEOMICINE/ZINC BACITRACINE
47 1NEOMYCIN & POLYMYXIN B SULFATES & BACITRACIN ZINC & HYDROCORTISONE
48 3NEOMYCIN AND POLYMYXIN B SULFATE
49 3NEOMYCIN AND POLYMYXIN B SULFATES AND BACITRACIN ZINC
50 3NEOMYCIN AND POLYMYXIN B SULFATES AND DEXAMETHASONE
51 4NEOMYCIN AND POLYMYXIN B SULFATES AND GRAMICIDIN
52 6NEOMYCIN AND POLYMYXIN B SULFATES AND HYDROCORTISONE
53 2NEOMYCIN AND POLYMYXIN B SULFATES, BACITRACIN ZINC AND HYDROCORTISONE
54 9NEOMYCIN SULFATE
55 1NEOMYCIN SULFATE AND DEXAMETHASONE SODIUM PHOSPHATE
56 1NEOMYCIN SULFATE AND POLYMYXIN B SULFATE GRAMICIDIN
57 1NEOMYCIN SULFATE, POLYMYXIN B SULFATE & HYDROCORTISONE
58 2NEOMYCIN SULFATE-DEXAMETHASONE SODIUM PHOSPHATE
59 2NEOMYCIN SULFATE-POLYMYXIN B SULFATE-HYDROCORTISONE
60 4NEOMYCIN SULFATE-TRIAMCINOLONE ACETONIDE
61 1NEOPRO 325
62 2NEOSPORIN
63 2NEOSPORIN G.U. IRRIGANT
64 1Naseptin
65 2Neocin
66 1Neocin 220
67 1Neocin 500
68 1Neocin M
69 1Neocin-700
70 1Neopol Vaginal Soft Capsule
71 1Ns-20
72 1ORIDERMYL
73 2OTICAIR
74 1OTOBIONE
75 2OTOCORT
76 1Otosporin
77 1PEDIOTIC
78 1POLY-PRED
79 1POLYGYNAX®
80 1SCOUR SUSPENSION
81 3STATROL
82 1Terfuzol
83 1Uniflex- N
84 1Videtrol
85 1ZINC BACITRACIN,NEOMYCIN SULFATE,POLYMYXIN B SULFATE & HYDROCORTISONE
86 10Blank
01 1Brazil
02 7Canada
03 3China
04 9India
05 3Italy
06 2Malaysia
07 1Poland
08 2Romania
09 4South Africa
10 9South Korea
11 2Turkey
12 114USA
13 2Vietnam
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : FML Neo Liquifilm Ophthalmic Suspension
Dosage Form : OPD
Dosage Strength : 5mg/ml
Packaging : 5X1mg/ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
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
Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.
Regulatory Info : Dossier Available
Registration Country : Poland
Brand Name :
Dosage Form : Suspension for Cutaneous Spray
Dosage Strength : 11.72MG/GM
Packaging :
Approval Date :
Application Number :
Regulatory Info : Dossier Available
Registration Country : Poland
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
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
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
Regulatory Info : DISCN
Registration Country : USA
HYDROCORTISONE; NEOMYCIN SULFATE
Brand Name : NEO-CORT-DOME
Dosage Form : CREAM;TOPICAL
Dosage Strength : 1%;EQ 3.5MG BASE/GM
Packaging :
Approval Date : 1984-06-05
Application Number : 50237
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
HYDROCORTISONE; NEOMYCIN SULFATE
Brand Name : NEO-CORT-DOME
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.5%;EQ 3.5MG BASE/GM
Packaging :
Approval Date : 1984-06-05
Application Number : 50237
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
ACETIC ACID, GLACIAL; HYDROCORTISONE; NEOMYCIN SULFATE
Brand Name : NEO-CORT-DOME
Dosage Form : SUSPENSION/DROPS;OTIC
Dosage Strength : 2%;1%;EQ 0.35% BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 50238
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NEOMYCIN SULFATE
Dosage Form : TABLET;ORAL
Dosage Strength : 500MG
Packaging :
Approval Date : 1982-01-01
Application Number : 60365
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
FLURANDRENOLIDE; NEOMYCIN SULFATE
Brand Name : CORDRAN N
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 0.05%;EQ 3.5MG BASE/GM
Packaging :
Approval Date : 1982-01-01
Application Number : 50345
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
FLURANDRENOLIDE; NEOMYCIN SULFATE
Brand Name : CORDRAN N
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.05%;EQ 3.5MG BASE/GM
Packaging :
Approval Date : 1982-01-01
Application Number : 50346
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NEOMYCIN SULFATE
Dosage Form : TABLET;ORAL
Dosage Strength : 500MG
Packaging :
Approval Date : 1982-01-01
Application Number : 60385
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
HYDROCORTISONE ACETATE; NEOMYCIN SULFATE
Brand Name : COR-OTICIN
Dosage Form : SUSPENSION/DROPS;OPHTHALMIC
Dosage Strength : 1.5%;EQ 3.5MG BASE/ML
Packaging :
Approval Date : 1982-01-01
Application Number : 60188
Regulatory Info : DISCN
Registration Country : USA
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
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
Regulatory Info : DISCN
Registration Country : USA
DEXAMETHASONE SODIUM PHOSPHATE; NEOMYCIN SULFATE
Brand Name : NEODECADRON
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.1% PHOSPHATE;EQ 3.5MG BASE/ML
Packaging :
Approval Date : 1982-01-01
Application Number : 50322
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
DEXAMETHASONE SODIUM PHOSPHATE; NEOMYCIN SULFATE
Brand Name : NEODECADRON
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : EQ 0.05% PHOSPHATE;EQ 3.5MG BASE/GM
Packaging :
Approval Date : 1982-01-01
Application Number : 50324
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
NEOMYCIN SULFATE; PREDNISOLONE SODIUM PHOSPHATE
Brand Name : NEO-HYDELTRASOL
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : EQ 3.5MG BASE/GM;EQ 0.25% PHOSPHATE
Packaging :
Approval Date : 1982-01-01
Application Number : 50378
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;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
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
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
Regulatory Info : DISCN
Registration Country : USA
Brand Name : MYCIFRADIN
Dosage Form : SOLUTION;ORAL
Dosage Strength : EQ 87.5MG BASE/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 50285
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NEOBIOTIC
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 350MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 60475
Regulatory Info : DISCN
Registration Country : USA
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 : RX
Registration Country : USA
Brand Name : NEOMYCIN SULFATE
Dosage Form : TABLET;ORAL
Dosage Strength : 500MG
Packaging :
Approval Date : 1982-01-01
Application Number : 60304
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
COLISTIN SULFATE; HYDROCORTISONE ACETATE; NEOMYCIN SULFATE; THONZONIUM BROMIDE
Brand Name : COLY-MYCIN S
Dosage Form : SUSPENSION/DROPS;OTIC
Dosage Strength : EQ 3MG BASE/ML;10MG/ML;EQ 3.3MG BASE/ML;0.5MG/ML
Packaging :
Approval Date : 1982-01-01
Application Number : 50356
Regulatory Info : RX
Registration Country : USA
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