01 1AbbVie Inc
02 52care4
03 1Abdi Ibrahim
04 2Actavis Inc
05 1Activo Health
06 8Alcon Inc
07 2Alembic Pharmaceuticals Limited
08 1Amneal Pharmaceuticals
09 4Apotex Inc
10 2Appasamy Associates
11 1Ascent Innovative Medicines
12 2Aurobindo Pharma Limited
13 1Aurolab
14 1Barr Laboratories
15 2Bausch & Lomb Incorporated
16 1Blumont Ofta Trading Ltd
17 1Cinfa
18 1Epione Medicine Aps
19 2FDC
20 1Farmigea
21 1Florida Pharmaceutical Products
22 3GLAND PHARMA LIMITED
23 1GSK
24 2Gen-Eye
25 12Glenmark Pharmaceuticals
26 1Greenco Biologicals
27 2Hanlim Pharmaceuticals Inc
28 1Hikma Pharmaceuticals
29 2Indoco Remedies Limited
30 2Juta Pharma Gmbh
31 2Kolmar Korea Co., Ltd.
32 1Labatec Pharm
33 2MINT PHARMACEUTICALS INC
34 1Misom Labs Ltd
35 1Misom Labs Ltd.
36 1Nobel Pharma Schweiz Ag
37 12Novartis Pharmaceuticals Corporation
38 5ORIFARM GROUP AS
39 3Opes Health Care
40 1Padagis
41 1Paranova Group AS
42 1Pharmascience Inc.
43 1Qualix Pharma Sl
44 2Rising Pharmaceuticals Inc
45 2SANIS HEALTH INC
46 3Sandoz B2B
47 2ScieGen Pharmaceuticals
48 2Somerset Pharmaceuticals Inc
49 1Tiedra Pharmaceuticals Sl
50 1UNIDO Pharmaceutical
51 1USV Private Limited
52 2Unimed Pharm Inc.
53 1Viatris
54 1Vir Sa Chemical And Pharmaceutical Industry
55 8World Medicine
56 1Zambon Switzerland
57 2Éticos
01 2Dropper Bottle
02 2EYE DROP
03 4EYE DROPS
04 11Eye Drop
05 12Eye Drop Solution
06 14Eye Drops
07 4Inhalation Spray
08 1NAS
09 2NASAL SPRAY
10 8Nasal Spray
11 3OPD
12 1OPHTHALMIC SOLUTION
13 1OPTHALMIC SOLUTION
14 8Ophthalmic Solution
15 1Ophthalmic Solution
16 9SOLUTION
17 29SOLUTION/DROPS;OPHTHALMIC
18 1SOLUTION; OPHTHALMIC
19 2SOLUTION;OPHTHALMIC
20 1SPRAY, METERED DOSE
21 6SPRAY, METERED;NASAL
22 2Solution
23 1Spray, Metered
24 1Suspension For Nasal Spray
25 1TAB
26 1Blank
01 3Allowed
02 8Approved
03 1Authorised
04 9Authorized
05 2Cancelled
06 7DISCN
07 13Generic
08 4Marketed
09 3Not Marketed
10 23OTC
11 2Originator
12 22Prescription
13 4RX
14 27Blank
01 1ALLERNIL-HS
02 1ALLERNIL-O
03 1Allergiol
04 1Allergiol Forte
05 1Apadin
06 1GB-OLA OD
07 1MINT-OLOPATADINE
08 1MINT-OLOPATADINE 0.2%
09 1Mometasone Furoate/Olopatadine Glenmark
10 1OLOGIC
11 1OLOPAGEN
12 1OLOPAGEN ONCE DAILY
13 2OLOPANOL
14 1OLOPATADINE
15 1OLOPATADINE 0.2%
16 33OLOPATADINE HYDROCHLORIDE
17 1OPT
18 1Olopatadin "Epione"
19 1Olopatadin "Juta"
20 1Olopatadin "Misom"
21 1Olopatadin "Orifarm"
22 1Olopatadin "Viatris"
23 1Olopatadina Cinfa
24 1Olopatadina Juta
25 1Olopatadina Vir
26 1Olopatadine Abamed
27 1Olopatadine Labatec
28 1Olopatadine Misom
29 1Olopatadine Orifarm
30 2Olopatadine Unimed Pharma
31 1Olotivo
32 14Opatanol
33 1Optamont
34 2PALLADA
35 1PALLADA-NS
36 1PATADAY
37 2PATADAY ONCE DAILY RELIEF
38 1PATADAY TWICE DAILY RELIEF
39 1PATANASE
40 1PATANOL
41 1PAZEO
42 1Pallada
43 1Pallada-NS
44 1Pata Eyen Drops
45 1Pata Once Drops
46 1Patadin
47 1Patanol
48 3RYALTRIS
49 10Ryaltris
50 1Ryaltris ?g ?g
51 1SANDOZ OLOPATADINE
52 1SANDOZ OLOPATADINE 0.2%
53 4Toredin
54 12Blank
01 1Bangladesh
02 11Canada
03 10Denmark
04 2Estonia
05 10India
06 2Italy
07 1Malta
08 5Moldova
09 7Norway
10 2Paraguay
11 5South Africa
12 5South Korea
13 11Spain
14 8Sweden
15 3Switzerland
16 7Turkey
17 38USA
Regulatory Info : Authorised
Registration Country : Malta
Brand Name : Olopatadine Unimed Pharma
Dosage Form : Eye Drop Solution
Dosage Strength : 1MG/ML
Packaging :
Approval Date : 2024-07-22
Application Number :
Regulatory Info : Authorised
Registration Country : Malta
Regulatory Info :
Registration Country : USA
Brand Name : OLOPATADINE HYDROCHLORIDE
Dosage Form : SOLUTION;OPHTHALMIC
Dosage Strength : 0.2%
Packaging :
Approval Date :
Application Number : 202526
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : OLOPATADINE HYDROCHLORIDE
Dosage Form : SOLUTION;OPHTHALMIC
Dosage Strength : 0.1%
Packaging :
Approval Date :
Application Number : 203416
Regulatory Info :
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
Brand Name : PATADAY TWICE DAILY RELIEF
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.1% BASE
Packaging :
Approval Date : 1996-12-18
Application Number : 20688
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
Brand Name : PATADAY ONCE DAILY RELIEF
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.2% BASE
Packaging :
Approval Date : 2004-12-22
Application Number : 21545
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
Brand Name : OLOPATADINE HYDROCHLORIDE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.1% BASE
Packaging :
Approval Date : 2015-12-07
Application Number : 78350
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
Brand Name : OLOPATADINE HYDROCHLORIDE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.2% BASE
Packaging :
Approval Date : 2017-12-05
Application Number : 90918
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : OLOPATADINE HYDROCHLORIDE
Dosage Form : SPRAY, METERED;NASAL
Dosage Strength : 0.665MG/SPRAY
Packaging :
Approval Date : 2014-10-08
Application Number : 91572
Regulatory Info : RX
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
Brand Name : OLOPATADINE HYDROCHLORIDE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.1% BASE
Packaging :
Approval Date : 2015-12-18
Application Number : 204812
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
Brand Name : OLOPATADINE HYDROCHLORIDE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.2% BASE
Packaging :
Approval Date : 2015-07-13
Application Number : 90848
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
Brand Name : OLOPATADINE HYDROCHLORIDE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.1% BASE
Packaging :
Approval Date : 2017-06-28
Application Number : 200810
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PATANASE
Dosage Form : SPRAY, METERED;NASAL
Dosage Strength : 0.665MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2008-04-15
Application Number : 21861
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : OLOPATADINE HYDROCHLORIDE
Dosage Form : SPRAY, METERED;NASAL
Dosage Strength : 0.665MG/SPRAY
Packaging :
Approval Date : 2017-01-31
Application Number : 202853
Regulatory Info : RX
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
Brand Name : OLOPATADINE HYDROCHLORIDE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.1% BASE
Packaging :
Approval Date : 2018-03-21
Application Number : 204392
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
Brand Name : OLOPATADINE HYDROCHLORIDE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.2% BASE
Packaging :
Approval Date : 2020-06-16
Application Number : 204620
Regulatory Info : OTC
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : OLOPATADINE HYDROCHLORIDE
Dosage Form : SOLUTION; OPHTHALMIC
Dosage Strength : 0.1%
Packaging :
Approval Date :
Application Number : 90972
Regulatory Info :
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : OLOPATADINE HYDROCHLORIDE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.1% BASE
Packaging :
Approval Date : 2017-01-10
Application Number : 204532
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : OLOPATADINE HYDROCHLORIDE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.2% BASE
Packaging :
Approval Date : 2017-12-05
Application Number : 204723
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
Brand Name : OLOPATADINE HYDROCHLORIDE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.1% BASE
Packaging :
Approval Date : 2015-12-07
Application Number : 203152
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : OLOPATADINE HYDROCHLORIDE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.1% BASE
Packaging :
Approval Date : 2015-12-07
Application Number : 204706
Regulatory Info : DISCN
Registration Country : USA
