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

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03 7Allergan Aesthetics
04 8Alfred E Tiefenbacher GmbH
05 4Pharmathen SA
06 1Mankind Pharma
07 62care4
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16 6Apotex Inc
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27 2Brown & Burk
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31 1EG Spa
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34 1FB VISION SPA
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36 2GLAND PHARMA LIMITED
37 1Gen-Eye
38 8Genetic Spa
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40 2Indiana Ophthalmics
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44 3Laboratoires Thea
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55 1S.C. Rompharm Company SRL
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57 11STADA Arzneimittel
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66 1Trinity Pharmaceuticals
67 4VISUfarma
68 3Viatris
69 3WAGNER PHARMACEUTICALS PTY LTD
70 4World Medicine
71 5Zentiva
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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 6Eye Drop; Eye Drop
09 16Eye Drops
10 14Eye Drops Solution
11 3Eye Drops Solution For Ophthalmic
12 1Eye DropsÂ
13 1Eye Gel
14 1Eye Gel
15 1Eye drop
16 1Eye/Ear Drop
17 1GEL;OPHTHALMIC
18 1IMPLANT;OPHTHALMIC
19 8OPD
20 3OPHTHALMIC SOLUTION
21 1Ophthalmic Gel
22 2Ophthalmic Gel In Single-Dose Container
23 16Ophthalmic 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 26Authorized
04 14Cancelled
05 3DISCN
06 6Deregistered
07 4EU Approved
08 11Generic
09 1Generic Dossiers Under Development For EU
10 9Marketed
11 4Originator
12 13Prescription
13 17RX
14 8Registered in EU
15 3Suspended
16 3Withdrawn
17 66Blank
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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 3Bimabloc
27 2Bimaprez
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 1Bimatoprost/Timolol Elvim
44 2Bimatoprost/Timolol Genetic
45 1Bimatoprost/Timolol Ratiopharm
46 1Bimatoprost/Timolol Sandoz
47 4Bimatoprost/Timolol Stada
48 3Bimatoprost/Timolol Teva
49 1Bimatoprost/Timolol Viatris
50 3Bimatoprost/Timolol Zentiva
51 1Bimeox
52 1Bimi
53 1Bimoptic Plus Rompharm
54 3Bimprozt
55 1Bimtim
56 3Bimtop
57 1Brinzolamid/Timolol Medical Valley
58 1Brinzolamide/Timolol Abacus Medicine
59 1Brinzolamide/Timolol Accord
60 1Brinzolamide/Timolol Azad
61 1Brinzolamide/Timolol Stada
62 1Brinzolamide/Timolol Zentiva
63 1Combigan
64 1DURYSTA
65 1Duelym
66 1Ecbirio
67 3Elymbus
68 1Elymbus g
69 1FREEDOM BIMATO- Eye drop 5ML
70 1GANFORT
71 3GANfort PF 0.3/5
72 1GLAUPTICO
73 14Ganfort
74 3Ganfort 0.3/5
75 1Ganfort Unit Dose
76 1Iricryn
77 2LATISSE
78 5LUMIGAN
79 1LUMIGAN 0.01%
80 1LUMIGAN RC
81 1Lasin
82 22Lumigan
83 1Lumigan 0.03%
84 3Lumigan PF
85 1Lumigan Unit Dose
86 1Timpromat
87 1VISTITAN
88 1VISUPLAIN
89 1Visublend
90 1Visuplain
91 1Vizibim
92 1Vizimaco
93 1ZIMED PF
94 1ZOLYMBUS
95 1Zimed
96 25Blank
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01 1Argentina
02 24Australia
03 7Canada
04 2China
05 9Estonia
06 8Germany
07 4Greece
08 8India
09 26Italy
10 3Malta
11 1Moldova
12 9Norway
13 8South Africa
14 43Spain
15 31Sweden
16 8Switzerland
17 4Turkey
18 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