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01 1USV Private Limited

02 1Abdi Ibrahim

03 2Actavis Inc

04 7Alcon Inc

05 2Alembic Pharmaceuticals Limited

06 1Amneal Pharmaceuticals

07 5Apotex Inc

08 2Appasamy Associates

09 1Ascent Innovative Medicines

10 2Aurobindo Pharma Limited

11 1Aurolab

12 1Barr Laboratories

13 2Bausch & Lomb Incorporated

14 1FDC

15 1Farmigea

16 1Florida Pharmaceutical Products

17 2GLAND PHARMA LIMITED

18 1GLENMARK SPECLT

19 3Glenmark Pharmaceuticals

20 1Greenco Biologicals

21 2Hanlim Pharmaceuticals Inc

22 1Hikma Pharmaceuticals

23 2Indoco Remedies Limited

24 1JAMP PHARMA

25 2Kolmar Korea Co., Ltd.

26 2MINT PHARMACEUTICALS INC

27 5Novartis Pharmaceuticals Corporation

28 1Novartis South Africa (Pty) Ltd

29 2ORIFARM GROUP AS

30 3Opes Health Care

31 1Padagis

32 1Pharmascience Inc.

33 2Rising Pharmaceuticals Inc

34 2SANIS HEALTH INC

35 3Sandoz B2B

36 2ScieGen Pharmaceuticals

37 1Somerset Pharmaceuticals Inc

38 1Unimed Pharm Inc.

39 6World Medicine

40 1Zambon Switzerland

41 2Éticos

42 3Blank

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PharmaCompass

01

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VMX
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothUSV offers custom peptide synthesis ranging from gram to multi-gram to multi-kilogram quantities.

Regulatory Info : OTC

Registration Country : USA

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

USV Private Limited

02

VMX
Not Confirmed
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VMX
Not Confirmed

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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03

VMX
Not Confirmed
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VMX
Not Confirmed

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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04

VMX
Not Confirmed
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VMX
Not Confirmed

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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05

VMX
Not Confirmed
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VMX
Not Confirmed

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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06

VMX
Not Confirmed
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VMX
Not Confirmed

OLOPATADINE HYDROCHLORIDE

Brand Name : PATADAY ONCE DAILY RELIEF

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.7% BASE

Packaging :

Approval Date : 2015-01-30

Application Number : 206276

Regulatory Info : OTC

Registration Country : USA

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07

VMX
Not Confirmed
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VMX
Not Confirmed

OLOPATADINE HYDROCHLORIDE

Brand Name : OLOPATADINE HYDROCHLORIDE

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.2% BASE

Packaging :

Approval Date : 2019-04-29

Application Number : 209420

Regulatory Info : OTC

Registration Country : USA

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08

VMX
Not Confirmed
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VMX
Not Confirmed

OLOPATADINE HYDROCHLORIDE

Brand Name : OLOPATADINE HYDROCHLORIDE

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.1% BASE

Packaging :

Approval Date : 2018-12-07

Application Number : 209919

Regulatory Info : OTC

Registration Country : USA

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09

VMX
Not Confirmed
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VMX
Not Confirmed

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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10

VMX
Not Confirmed
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VMX
Not Confirmed

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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11

VMX
Not Confirmed
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VMX
Not Confirmed

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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12

VMX
Not Confirmed
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VMX
Not Confirmed

OLOPATADINE HYDROCHLORIDE

Brand Name : OLOPATADINE HYDROCHLORIDE

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.7% BASE

Packaging :

Approval Date :

Application Number : 209015

Regulatory Info :

Registration Country : USA

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13

VMX
Not Confirmed
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VMX
Not Confirmed

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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14

VMX
Not Confirmed
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VMX
Not Confirmed

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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15

VMX
Not Confirmed
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VMX
Not Confirmed

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 : DISCN

Registration Country : USA

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16

VMX
Not Confirmed
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VMX
Not Confirmed

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 : 206087

Regulatory Info : DISCN

Registration Country : USA

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17

VMX
Not Confirmed
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VMX
Not Confirmed

OLOPATADINE HYDROCHLORIDE

Brand Name : OLOPATADINE HYDROCHLORIDE

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.1% BASE

Packaging :

Approval Date : 2019-09-26

Application Number : 209282

Regulatory Info : DISCN

Registration Country : USA

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18

VMX
Not Confirmed
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VMX
Not Confirmed

OLOPATADINE HYDROCHLORIDE

Brand Name : OLOPATADINE HYDROCHLORIDE

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.7% BASE

Packaging :

Approval Date : 2020-02-19

Application Number : 208637

Regulatory Info : DISCN

Registration Country : USA

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19

VMX
Not Confirmed
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VMX
Not Confirmed

OLOPATADINE HYDROCHLORIDE

Brand Name : OLOPATADINE HYDROCHLORIDE

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.1% BASE

Packaging :

Approval Date : 2019-08-02

Application Number : 209619

Regulatory Info : OTC

Registration Country : USA

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20

VMX
Not Confirmed
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VMX
Not Confirmed

OLOPATADINE HYDROCHLORIDE

Brand Name : OLOPATADINE HYDROCHLORIDE

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.2% BASE

Packaging :

Approval Date : 2020-05-20

Application Number : 209752

Regulatory Info : OTC

Registration Country : USA

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21

VMX
Not Confirmed
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VMX
Not Confirmed

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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22

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VMX
Not Confirmed

OLOPATADINE HYDROCHLORIDE

Brand Name : PATANASE

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.665MG/SPRAY

Packaging :

Approval Date : 2008-04-15

Application Number : 21861

Regulatory Info : DISCN

Registration Country : USA

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23

VMX
Not Confirmed
arrow
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VMX
Not Confirmed

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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24

VMX
Not Confirmed
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VMX
Not Confirmed

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 : DISCN

Registration Country : USA

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25

VMX
Not Confirmed
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VMX
Not Confirmed

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 : DISCN

Registration Country : USA

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26

VMX
Not Confirmed
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VMX
Not Confirmed

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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27

VMX
Not Confirmed
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VMX
Not Confirmed

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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28

VMX
Not Confirmed
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VMX
Not Confirmed

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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29

VMX
Not Confirmed
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VMX
Not Confirmed

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 : 206306

Regulatory Info : OTC

Registration Country : USA

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30

VMX
Not Confirmed
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VMX
Not Confirmed

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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