01 12care4
02 1Abdi Ibrahim
03 2Actavis Inc
04 1Activo Health
05 10Alcon Inc
06 2Alembic Pharmaceuticals Limited
07 1Amneal Pharmaceuticals
08 4Apotex Inc
09 2Appasamy Associates
10 1Ascent Innovative Medicines
11 2Aurobindo Pharma Limited
12 1Aurolab
13 1Barr Laboratories
14 2Bausch & Lomb Incorporated
15 1Blumont Ofta Trading Ltd
16 1Cinfa
17 2FDC
18 1Farmigea
19 1Florida Pharmaceutical Products
20 2GLAND PHARMA LIMITED
21 1GSK
22 2Gen-Eye
23 7Glenmark Pharmaceuticals
24 1Greenco Biologicals
25 2Hanlim Pharmaceuticals Inc
26 1Hikma Pharmaceuticals
27 2Indoco Remedies Limited
28 1Juta Pharma Gmbh
29 2Kolmar Korea Co., Ltd.
30 1Labatec Pharm
31 2MINT PHARMACEUTICALS INC
32 1Misom Labs Ltd.
33 1Nobel Pharma Schweiz Ag
34 7Novartis Pharmaceuticals Corporation
35 1Novartis South Africa (Pty) Ltd
36 3ORIFARM GROUP AS
37 3Opes Health Care
38 1Padagis
39 1Pharmascience Inc.
40 1Qualix Pharma Sl
41 2Rising Pharmaceuticals Inc
42 2SANIS HEALTH INC
43 3Sandoz B2B
44 2ScieGen Pharmaceuticals
45 2Somerset Pharmaceuticals Inc
46 1Tiedra Pharmaceuticals Sl
47 1UNIDO Pharmaceutical
48 1USV Private Limited
49 1Unimed Pharm Inc.
50 1Vir Sa Chemical And Pharmaceutical Industry
51 6World Medicine
52 1Zambon Switzerland
53 2Éticos
01 2Dropper Bottle
02 2EYE DROP
03 4EYE DROPS
04 11Eye Drop
05 11Eye 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 9Authorized
04 2Cancelled
05 7DISCN
06 13Generic
07 22OTC
08 2Originator
09 10Prescription
10 4RX
11 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 1Olotivo
26 12Opatanol
27 1Optamont
28 2PALLADA
29 1PALLADA-NS
30 1PATADAY
31 2PATADAY ONCE DAILY RELIEF
32 1PATADAY TWICE DAILY RELIEF
33 1PATANASE
34 1PATANOL
35 1PAZEO
36 1Pata Eyen Drops
37 1Pata Once Drops
38 1Patadin
39 1Patanol
40 3RYALTRIS
41 2Ryaltris
42 1Ryaltris ?g ?g
43 1SANDOZ OLOPATADINE
44 1SANDOZ OLOPATADINE 0.2%
45 1Toredin
46 12Blank
01 1Bangladesh
02 11Canada
03 10India
04 2Italy
05 4Norway
06 2Paraguay
07 5South Africa
08 5South Korea
09 11Spain
10 7Sweden
11 3Switzerland
12 7Turkey
13 37USA
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 : 2017-07-26
Application Number : 206046
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
