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01 12care4

02 1Abdi Ibrahim

03 2Actavis Inc

04 1Activo Health

05 6Alcon 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 2FDC

17 1Farmigea

18 1Florida Pharmaceutical Products

19 2GLAND PHARMA LIMITED

20 2Gen-Eye

21 5Glenmark Pharmaceuticals

22 1Greenco Biologicals

23 2Hanlim Pharmaceuticals Inc

24 1Hikma Pharmaceuticals

25 2Indoco Remedies Limited

26 1JAMP PHARMA

27 2Kolmar Korea Co., Ltd.

28 1Labatec Pharm

29 2MINT PHARMACEUTICALS INC

30 1Misom Labs Ltd.

31 6Novartis Pharmaceuticals Corporation

32 1Novartis South Africa (Pty) Ltd

33 3ORIFARM GROUP AS

34 3Opes Health Care

35 1Padagis

36 1Pharmascience Inc.

37 2Rising Pharmaceuticals Inc

38 2SANIS HEALTH INC

39 3Sandoz B2B

40 2ScieGen Pharmaceuticals

41 2Somerset Pharmaceuticals Inc

42 1UNIDO Pharmaceutical

43 1USV Private Limited

44 1Unimed Pharm Inc.

45 6World Medicine

46 1Zambon Switzerland

47 2Éticos

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PharmaCompass

01

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OLOPATADINE HYDROCHLORIDE

Brand Name : OLOPATADINE HYDROCHLORIDE

Dosage Form : SOLUTION;OPHTHALMIC

Dosage Strength : 0.2%

Packaging :

Approval Date :

Application Number : 202526

Regulatory Info :

Registration Country : USA

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02

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OLOPATADINE HYDROCHLORIDE

Brand Name : OLOPATADINE HYDROCHLORIDE

Dosage Form : SOLUTION;OPHTHALMIC

Dosage Strength : 0.1%

Packaging :

Approval Date :

Application Number : 203416

Regulatory Info :

Registration Country : USA

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03

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OLOPATADINE HYDROCHLORIDE

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

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04

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OLOPATADINE HYDROCHLORIDE

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

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05

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OLOPATADINE HYDROCHLORIDE

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

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06

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OLOPATADINE HYDROCHLORIDE

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

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07

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OLOPATADINE HYDROCHLORIDE

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

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08

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OLOPATADINE HYDROCHLORIDE

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

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09

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OLOPATADINE HYDROCHLORIDE

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

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10

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OLOPATADINE HYDROCHLORIDE

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

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11

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OLOPATADINE HYDROCHLORIDE

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

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12

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OLOPATADINE HYDROCHLORIDE

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

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13

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OLOPATADINE HYDROCHLORIDE

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

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14

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OLOPATADINE HYDROCHLORIDE

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

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15

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OLOPATADINE HYDROCHLORIDE

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

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16

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OLOPATADINE HYDROCHLORIDE

Brand Name : OLOPATADINE HYDROCHLORIDE

Dosage Form : SOLUTION; OPHTHALMIC

Dosage Strength : 0.1%

Packaging :

Approval Date :

Application Number : 90972

Regulatory Info :

Registration Country : USA

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17

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OLOPATADINE HYDROCHLORIDE

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

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18

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OLOPATADINE HYDROCHLORIDE

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

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19

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OLOPATADINE HYDROCHLORIDE

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

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20

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OLOPATADINE HYDROCHLORIDE

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

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