01 1AbbVie Inc
02 12care4
03 1Abdi Ibrahim
04 2Actavis Inc
05 1Activo Health
06 10Alcon 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 2FDC
19 1Farmigea
20 1Florida Pharmaceutical Products
21 2GLAND PHARMA LIMITED
22 1GSK
23 2Gen-Eye
24 7Glenmark Pharmaceuticals
25 1Greenco Biologicals
26 2Hanlim Pharmaceuticals Inc
27 1Hikma Pharmaceuticals
28 2Indoco Remedies Limited
29 1Juta Pharma Gmbh
30 2Kolmar Korea Co., Ltd.
31 1Labatec Pharm
32 2MINT PHARMACEUTICALS INC
33 1Misom Labs Ltd.
34 1Nobel Pharma Schweiz Ag
35 7Novartis Pharmaceuticals Corporation
36 1Novartis South Africa (Pty) Ltd
37 3ORIFARM GROUP AS
38 3Opes Health Care
39 1Padagis
40 1Pharmascience Inc.
41 1Qualix Pharma Sl
42 2Rising Pharmaceuticals Inc
43 2SANIS HEALTH INC
44 3Sandoz B2B
45 2ScieGen Pharmaceuticals
46 2Somerset Pharmaceuticals Inc
47 1Tiedra Pharmaceuticals Sl
48 1UNIDO Pharmaceutical
49 1USV Private Limited
50 1Unimed Pharm Inc.
51 1Vir Sa Chemical And Pharmaceutical Industry
52 6World Medicine
53 1Zambon Switzerland
54 2Éticos
01 2Dropper Bottle
02 2EYE DROP
03 4EYE DROPS
04 11Eye Drop
05 12Eye Drop Solution
06 1Eye Drops
07 4Eye drops, resolution
08 3Inhalation Spray
09 1NAS
10 2NASAL SPRAY
11 3OPD
12 1OPHTHALMIC SOLUTION
13 1OPTHALMIC SOLUTION
14 5Ophthalmic Solution
15 1Ophthalmic Solution
16 9SOLUTION
17 28SOLUTION/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 7Approved
03 1Authorised
04 9Authorized
05 2Cancelled
06 7DISCN
07 13Generic
08 22OTC
09 2Originator
10 10Prescription
11 4RX
12 26Blank
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 32OLOPATADINE HYDROCHLORIDE
17 1OPT
18 1Olopatadina Cinfa
19 1Olopatadina Juta
20 1Olopatadina Vir
21 1Olopatadine Abamed
22 1Olopatadine Labatec
23 1Olopatadine Misom
24 1Olopatadine Orifarm
25 1Olopatadine Unimed Pharma
26 1Olotivo
27 12Opatanol
28 1Optamont
29 2PALLADA
30 1PALLADA-NS
31 1PATADAY
32 2PATADAY ONCE DAILY RELIEF
33 1PATADAY TWICE DAILY RELIEF
34 1PATANASE
35 1PATANOL
36 1PAZEO
37 1Pata Eyen Drops
38 1Pata Once Drops
39 1Patadin
40 1Patanol
41 3RYALTRIS
42 2Ryaltris
43 1Ryaltris ?g ?g
44 1SANDOZ OLOPATADINE
45 1SANDOZ OLOPATADINE 0.2%
46 1Toredin
47 12Blank
01 1Bangladesh
02 11Canada
03 10India
04 2Italy
05 1Malta
06 4Norway
07 2Paraguay
08 5South Africa
09 5South Korea
10 11Spain
11 7Sweden
12 3Switzerland
13 7Turkey
14 37USA
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
