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01 3ATENOLOL

02 3CARBAMAZEPINE

03 4CETIRIZINE HYDROCHLORIDE

04 3CIPROFLOXACIN HYDROCHLORIDE

05 3CLOMIPRAMINE HYDROCHLORIDE

06 3DICLOFENAC SODIUM

07 5DOXEPIN HYDROCHLORIDE

08 4ENALAPRIL MALEATE

09 1FEXOFENADINE HYDROCHLORIDE

10 3GLIPIZIDE

11 2LITHIUM CARBONATE

12 1LORATADINE

13 3OXYBUTYNIN CHLORIDE

14 2TOLTERODINE TARTRATE

15 4VENLAFAXINE HYDROCHLORIDE

16 1VERARD

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PharmaCompass

01

Brand Name : ATENOLOL

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : ATENOLOL

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Unique Biotech Limited

Dosage Form : TABLET; ORAL

Proprietary Name : ATENOLOL

Dosage Strength : 25MG

Approval Date : 2006-09-13

Application Number : 77443

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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02

Brand Name : ATENOLOL

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Brand Name : ATENOLOL

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Unique Biotech Limited

Dosage Form : TABLET; ORAL

Proprietary Name : ATENOLOL

Dosage Strength : 50MG

Approval Date : 2006-09-13

Application Number : 77443

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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03

Brand Name : ATENOLOL

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Brand Name : ATENOLOL

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Unique Biotech Limited

Dosage Form : TABLET; ORAL

Proprietary Name : ATENOLOL

Dosage Strength : 100MG

Approval Date : 2006-09-13

Application Number : 77443

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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04

Brand Name : CARBAMAZEPINE

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Brand Name : CARBAMAZEPINE

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Unique Biotech Limited

Dosage Form : TABLET, EXTENDED RELEASE; ORAL

Proprietary Name : CARBAMAZEPINE

Dosage Strength : 100MG

Approval Date : 2020-04-24

Application Number : 211623

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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05

Brand Name : CARBAMAZEPINE

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Brand Name : CARBAMAZEPINE

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Unique Biotech Limited

Dosage Form : TABLET, EXTENDED RELEASE; ORAL

Proprietary Name : CARBAMAZEPINE

Dosage Strength : 200MG

Approval Date : 2020-04-24

Application Number : 211623

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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06

Brand Name : CARBAMAZEPINE

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Brand Name : CARBAMAZEPINE

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Unique Biotech Limited

Dosage Form : TABLET, EXTENDED RELEASE; ORAL

Proprietary Name : CARBAMAZEPINE

Dosage Strength : 400MG

Approval Date : 2020-04-24

Application Number : 211623

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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07

Brand Name : CETIRIZINE HYDROCHLO...

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Brand Name : CETIRIZINE HYDROCHLO...

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Unique Biotech Limited

Dosage Form : TABLET; ORAL

Proprietary Name : CETIRIZINE HYDROCHLORIDE...

Dosage Strength : 5MG

Approval Date : 2009-08-26

Application Number : 77829

RX/OTC/DISCN : OTC

RLD : No

TE Code :

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08

Brand Name : CETIRIZINE HYDROCHLO...

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Brand Name : CETIRIZINE HYDROCHLO...

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Unique Biotech Limited

Dosage Form : TABLET; ORAL

Proprietary Name : CETIRIZINE HYDROCHLORIDE...

Dosage Strength : 10MG

Approval Date : 2009-08-26

Application Number : 77829

RX/OTC/DISCN : OTC

RLD : No

TE Code :

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09

Brand Name : CETIRIZINE HYDROCHLO...

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Brand Name : CETIRIZINE HYDROCHLO...

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Unique Biotech Limited

Dosage Form : TABLET; ORAL

Proprietary Name : CETIRIZINE HYDROCHLORIDE...

Dosage Strength : 5MG

Approval Date : 2009-08-26

Application Number : 77829

RX/OTC/DISCN : OTC

RLD : No

TE Code :

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10

Brand Name : CETIRIZINE HYDROCHLO...

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Brand Name : CETIRIZINE HYDROCHLO...

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Unique Biotech Limited

Dosage Form : TABLET; ORAL

Proprietary Name : CETIRIZINE HYDROCHLORIDE...

Dosage Strength : 10MG

Approval Date : 2009-08-26

Application Number : 77829

RX/OTC/DISCN : OTC

RLD : No

TE Code :

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