European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

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01 1Polpharma
02 34AbbVie Inc
03 13Allergan Aesthetics
04 8Alfred E Tiefenbacher GmbH
05 4Pharmathen SA
06 1Mankind Pharma
07 12care4
08 1AEQUUS PHARMACEUTICALS INC.
09 1AZAD Pharma
10 1Abacus Medicine
11 5Accord healthcare
12 2Alembic Pharmaceuticals Limited
13 3Alphapharm PTY Ltd
14 1Amneal Pharmaceuticals
15 2Apotex Fermentation Inc.
16 6Apotex Inc
17 1Appasamy Associates
18 2Aristo Pharma GmbH
19 1Aurobindo Pharma Limited
20 2Austell Laboratories
21 2Bausch & Lomb Incorporated
22 1Biogaran
23 2Blumont Ofta Trading Ltd
24 2Brill Pharma Sl
25 1Brooks laboratories Limited
26 2Brown & Burk
27 1DIFARMED S.L.
28 3DOC Generici
29 1Dari Pharma Sl
30 1EG Spa
31 1EQL Pharma
32 2Ebb Medical
33 1FB VISION SPA
34 1Freedom Biopharma
35 2GLAND PHARMA LIMITED
36 1Gen-Eye
37 8Genetic Spa
38 2Hikma Pharmaceuticals
39 2Indiana Ophthalmics
40 3Indoco Remedies Limited
41 2Jiangsu Hengrui Medicine
42 1Labatec Pharm
43 3Laboratoires Thea
44 1Laboratorios Poen
45 1Laboratorios Salvat
46 1Lupin Ltd
47 1Medical Valley
48 1Medicom Healthcare
49 1Mepha Pharma
50 2Micro Labs Limited
51 1Neuraxpharm
52 3Pharmascience Inc.
53 1Ratiopharm Espana Sa
54 2SIFI
55 11STADA Arzneimittel
56 15Sandoz B2B
57 1Somerset Pharmaceuticals Inc
58 3Teva Pharmaceutical Industries
59 1Thea Laboratories
60 1Thea Pharma
61 1Thea Pharma Sa
62 1Tiedra Pharmaceuticals Sl
63 4VISUfarma
64 2Viatris
65 3WAGNER PHARMACEUTICALS PTY LTD
66 4World Medicine
67 4Zentiva
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01 1Bimatoprost 0,3Mg/Ml 0.4 Ml 30Units Solution Ophthalmic Use
02 1Bimatoprost 0,3Mg/Ml 3Ml Solution Ophthalmic Use
03 1Bimatoprost 0.1Mg/Ml 3Ml Solution Ophthalmic Use
04 4EYE DROPS
05 36Eye Drop
06 8Eye Drop In Solution In Single-Dose Container
07 20Eye Drop Solution
08 8Eye Drops
09 14Eye Drops Solution
10 3Eye Drops Solution For Ophthalmic
11 1Eye Gel
12 1Eye drop
13 6Eye drops, resolution
14 1Eye drops, solution in dose container
15 2Eye gel in a dose container
16 1Eye/Ear Drop
17 1GEL;OPHTHALMIC
18 1IMPLANT;OPHTHALMIC
19 5OPD
20 3OPHTHALMIC SOLUTION
21 1Ophthalmic Gel
22 1Ophthalmic Gel In Single-Dose Container
23 7Ophthalmic Solution
24 4SOLUTION
25 15SOLUTION/DROPS;OPHTHALMIC
26 5SOLUTION/DROPS;TOPICAL
27 2SOLUTION; OPHTHALMIC
28 1SOLUTION;OPHTHALMIC
29 27Solution
30 1Timolol+Bimatoprost 300Mcg/Ml+5Mg/Ml 30 Joined' Solution Ophthalmic Use
31 1Timolol+Bimatoprost 900Mcg+15Mg Solution Ophthalmic Use
32 15eye drops
33 3Blank
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01 8Allowed
02 25Approved
03 25Authorized
04 14Cancelled
05 3DISCN
06 6Deregistered
07 4EU Approved
08 10Generic
09 1Generic Dossiers Under Development For EU
10 2Originator
11 4Prescription
12 17RX
13 8Registered in EU
14 3Suspensed
15 3Withdrawn
16 68Blank
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01 1Abiprost
02 1Amiriox
03 1BIALVIZ
04 2BIMADOC
05 1BIMAGAN
06 1BIMANEXT
07 1BIMAPRES 0,03%
08 1BIMAPRES 0.01%
09 1BIMASOPT
10 20BIMATOPROST
11 1BIMATOPROST AND TIMOLOL TEVA
12 1BIMATOPROST AND TIMOLOL ZENTIVA
13 1BIMATOPROST MYLAN
14 1BIMATOPROST SANDOZ GMBH
15 1BIMATOPROST TIMOLOL EG
16 1BIMATOPROST TIMOLOL MYLAN
17 1BIMATOPROST TIMOLOL SANDOZ
18 3BIMATOPROST-WGR
19 1BIMPOST
20 1BLEND VIEW
21 2BRINUS
22 1BROSTIMAB
23 1BYZANTIM
24 1Bamixol
25 1Bapiri
26 1Bimabloc
27 1Bimaprez
28 1Bimatoprost
29 4Bimatoprost Accord
30 2Bimatoprost Apotex
31 2Bimatoprost Aristo
32 1Bimatoprost Brown & Burk
33 1Bimatoprost Dari Pharma
34 1Bimatoprost Ebb
35 2Bimatoprost Genetic
36 1Bimatoprost Labatec
37 1Bimatoprost Qualigen
38 6Bimatoprost Sandoz
39 6Bimatoprost Stada
40 1Bimatoprost-Mepha Plus
41 1Bimatoprost/Timolol Biogaran
42 1Bimatoprost/Timolol Brown & Burk
43 2Bimatoprost/Timolol Genetic
44 1Bimatoprost/Timolol Ratiopharm
45 1Bimatoprost/Timolol Sandoz
46 4Bimatoprost/Timolol Stada
47 2Bimatoprost/Timolol Teva
48 2Bimatoprost/Timolol Zentiva
49 1Bimeox
50 1Bimi
51 3Bimprozt
52 1Bimtim
53 3Bimtop
54 1Brinzolamid/Timolol Medical Valley
55 1Brinzolamide/Timolol Abacus Medicine
56 1Brinzolamide/Timolol Accord
57 1Brinzolamide/Timolol Azad
58 1Brinzolamide/Timolol Stada
59 1Brinzolamide/Timolol Zentiva
60 1DURYSTA
61 1Ecbirio
62 4Elymbus
63 1Elymbus g
64 1FREEDOM BIMATO- Eye drop 5ML
65 1GANFORT
66 1GLAUPTICO
67 10Ganfort
68 1Ganfort Unit Dose
69 1Iricryn
70 2LATISSE
71 5LUMIGAN
72 1LUMIGAN 0.01%
73 1LUMIGAN RC
74 1Lasin
75 22Lumigan
76 1Lumigan 0.03%
77 3Lumigan PF
78 1Lumigan Unit Dose
79 1VISTITAN
80 1VISUPLAIN
81 1Visublend
82 1Visuplain
83 1Vizibim
84 1Vizimaco
85 1ZIMED PF
86 1ZOLYMBUS
87 1Zimed
88 25Blank
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01 1Argentina
02 18Australia
03 7Canada
04 2China
05 8Germany
06 4Greece
07 8India
08 26Italy
09 3Malta
10 9Norway
11 5South Africa
12 42Spain
13 31Sweden
14 8Switzerland
15 4Turkey
16 25USA
European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Iricryn
Dosage Form : Eye Drop
Dosage Strength : 0.3mg/ml
Packaging :
Approval Date : 13/06/2022
Application Number : 20210526000062
Regulatory Info : Approved
Registration Country : Sweden
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Regulatory Info : DISCN
Registration Country : USA
Brand Name : LUMIGAN
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 0.03% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2001-03-16
Application Number : 21275
Regulatory Info : DISCN
Registration Country : USA
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Regulatory Info :
Registration Country : Italy
Brand Name : Lumigan
Dosage Form : Bimatoprost 0.1Mg/Ml 3Ml Solution Ophthalmic Use
Dosage Strength : EYE DROPS 3 ml 0. 1 mg/ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info : Registered in EU
Registration Country : Germany
Brand Name :
Dosage Form : Solution
Dosage Strength : 0.1MG/ML
Packaging :
Approval Date :
Application Number :
Regulatory Info : Registered in EU
Registration Country : Germany
Pharmathen provides life cycle Management solutions for branded pharma, as well as to develop & establish new technology platforms.
Regulatory Info : EU Approved
Registration Country : Greece
Brand Name :
Dosage Form : Eye Drops Solution
Dosage Strength : 0.1MG/ML
Packaging :
Approval Date :
Application Number :
Regulatory Info : EU Approved
Registration Country : Greece
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
Regulatory Info : RX
Registration Country : USA
Brand Name : BIMATOPROST
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 0.01%
Packaging :
Approval Date : 2025-03-17
Application Number : 218196
Regulatory Info : RX
Registration Country : USA
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Regulatory Info : RX
Registration Country : USA
Brand Name : LUMIGAN
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 0.01%
Packaging :
Approval Date : 2010-08-31
Application Number : 22184
Regulatory Info : RX
Registration Country : USA
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Regulatory Info : RX
Registration Country : USA
Brand Name : LATISSE
Dosage Form : SOLUTION/DROPS;TOPICAL
Dosage Strength : 0.03%
Packaging :
Approval Date : 2008-12-24
Application Number : 22369
Regulatory Info : RX
Registration Country : USA
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Regulatory Info : RX
Registration Country : USA
Brand Name : DURYSTA
Dosage Form : IMPLANT;OPHTHALMIC
Dosage Strength : 10MCG
Packaging :
Approval Date : 2020-03-04
Application Number : 211911
Regulatory Info : RX
Registration Country : USA
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Regulatory Info :
Registration Country : Italy
Brand Name : LUMIGAN
Dosage Form : Eye Drops Solution For Ophthalmic
Dosage Strength : 0.1 mg/ml
Packaging : 3 ML 0.1 MG/ML - OPHTHALMIC USE SOLUTION
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
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Regulatory Info :
Registration Country : Italy
Brand Name : LUMIGAN
Dosage Form : Eye Drops Solution For Ophthalmic
Dosage Strength : 0.3 mg/ml
Packaging : 30 UNITS 0.4 ML 0.3 MG/ML - OPHTHALMIC USE SOLUTION
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
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Regulatory Info :
Registration Country : Italy
Brand Name : GANFORT
Dosage Form : Eye Drops
Dosage Strength : 0.3 mg/ml + 5 mg/ml
Packaging : 3 ML 0.3 MG/ML + 5 MG/ML - OPHTHALMIC USE SOLUTION
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
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Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Lumigan
Dosage Form : Eye Drop
Dosage Strength : 0.1mg/ml
Packaging :
Approval Date : 07/01/2010
Application Number : 20080416000058
Regulatory Info : Approved
Registration Country : Sweden
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Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Lumigan
Dosage Form : Eye Drop
Dosage Strength : 0.3mg/ml
Packaging :
Approval Date : 08/03/2002
Application Number : 20020308000094
Regulatory Info : Approved
Registration Country : Sweden
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Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Lumigan
Dosage Form : Eye Drop
Dosage Strength : 0.3mg/ml
Packaging :
Approval Date : 19/11/2012
Application Number : 20121206000060
Regulatory Info : Approved
Registration Country : Sweden
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Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Lumigan
Dosage Form : Eye Drop
Dosage Strength : 0.3mg/ml/ml
Packaging :
Approval Date : 31/05/2002
Application Number : 55918
Regulatory Info : Allowed
Registration Country : Switzerland
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Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Lumigan
Dosage Form : Eye Drop
Dosage Strength : 0.1mg/ml
Packaging :
Approval Date : 31/05/2002
Application Number : 55918
Regulatory Info : Allowed
Registration Country : Switzerland
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Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Lumigan Unit Dose
Dosage Form : Eye Drop
Dosage Strength : 0.3mg/ml
Packaging :
Approval Date : 12/07/2013
Application Number : 63092
Regulatory Info : Allowed
Registration Country : Switzerland
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Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Ganfort
Dosage Form : Eye Drop
Dosage Strength : 0.3mg/ml;5mg/ml
Packaging :
Approval Date : 19/05/2006
Application Number : 20050706000013
Regulatory Info : Approved
Registration Country : Sweden
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Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Ganfort
Dosage Form : Eye Drop
Dosage Strength : 0.3mg/ml;5mg/ml
Packaging :
Approval Date : 30/05/2013
Application Number : 20130706000036
Regulatory Info : Approved
Registration Country : Sweden