Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
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 3Accord 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 14Sandoz 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
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 17Eye 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
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 15RX
13 8Registered in EU
14 3Suspensed
15 70Blank
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 2Bimatoprost Accord
29 2Bimatoprost Apotex
30 2Bimatoprost Aristo
31 1Bimatoprost Brown & Burk
32 1Bimatoprost Dari Pharma
33 1Bimatoprost Ebb
34 2Bimatoprost Genetic
35 1Bimatoprost Labatec
36 1Bimatoprost Qualigen
37 6Bimatoprost Sandoz
38 6Bimatoprost Stada
39 1Bimatoprost-Mepha Plus
40 1Bimatoprost/Timolol Biogaran
41 1Bimatoprost/Timolol Brown & Burk
42 2Bimatoprost/Timolol Genetic
43 1Bimatoprost/Timolol Ratiopharm
44 1Bimatoprost/Timolol Sandoz
45 4Bimatoprost/Timolol Stada
46 2Bimatoprost/Timolol Teva
47 2Bimatoprost/Timolol Zentiva
48 1Bimeox
49 1Bimi
50 3Bimprozt
51 1Bimtim
52 3Bimtop
53 1Brinzolamid/Timolol Medical Valley
54 1Brinzolamide/Timolol Abacus Medicine
55 1Brinzolamide/Timolol Accord
56 1Brinzolamide/Timolol Azad
57 1Brinzolamide/Timolol Stada
58 1Brinzolamide/Timolol Zentiva
59 1DURYSTA
60 1Ecbirio
61 4Elymbus
62 1Elymbus g
63 1FREEDOM BIMATO- Eye drop 5ML
64 1GANFORT
65 1GLAUPTICO
66 10Ganfort
67 1Ganfort Unit Dose
68 1Iricryn
69 2LATISSE
70 5LUMIGAN
71 1LUMIGAN 0.01%
72 1LUMIGAN RC
73 1Lasin
74 22Lumigan
75 1Lumigan 0.03%
76 3Lumigan PF
77 1Lumigan Unit Dose
78 1VISTITAN
79 1VISUPLAIN
80 1Visublend
81 1Visuplain
82 1Vizibim
83 1Vizimaco
84 1ZIMED PF
85 1ZOLYMBUS
86 1Zimed
87 25Blank
01 1Argentina
02 18Australia
03 7Canada
04 2China
05 8Germany
06 4Greece
07 8India
08 26Italy
09 9Norway
10 5South Africa
11 42Spain
12 31Sweden
13 8Switzerland
14 4Turkey
15 25USA
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies 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
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
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
We are the TIEFENBACHER GROUP, Health Pioneers since 1963.
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
