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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

Pharmtech & Ingredients
Not Confirmed
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Brand Name : ATENOLOL

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Pharmtech & Ingredients
Not Confirmed

Unique Biotech Limited

Dosage Form : TABLET;ORAL

Brand Name : ATENOLOL

Dosage Strength : 25MG

Packaging :

Approval Date : 2006-09-13

Application Number : 77443

Regulatory Info : RX

Registration Country : USA

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02

Brand Name : ATENOLOL

Pharmtech & Ingredients
Not Confirmed
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Brand Name : ATENOLOL

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Pharmtech & Ingredients
Not Confirmed

Unique Biotech Limited

Dosage Form : TABLET;ORAL

Brand Name : ATENOLOL

Dosage Strength : 50MG

Packaging :

Approval Date : 2006-09-13

Application Number : 77443

Regulatory Info : RX

Registration Country : USA

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03

Brand Name : ATENOLOL

Pharmtech & Ingredients
Not Confirmed
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Brand Name : ATENOLOL

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Pharmtech & Ingredients
Not Confirmed

Unique Biotech Limited

Dosage Form : TABLET;ORAL

Brand Name : ATENOLOL

Dosage Strength : 100MG

Packaging :

Approval Date : 2006-09-13

Application Number : 77443

Regulatory Info : RX

Registration Country : USA

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04

Brand Name : CARBAMAZEPINE

Pharmtech & Ingredients
Not Confirmed
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Brand Name : CARBAMAZEPINE

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Pharmtech & Ingredients
Not Confirmed

Unique Biotech Limited

Dosage Form : TABLET, EXTENDED RELEASE...

Brand Name : CARBAMAZEPINE

Dosage Strength : 100MG

Packaging :

Approval Date : 2020-04-24

Application Number : 211623

Regulatory Info : RX

Registration Country : USA

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05

Brand Name : CARBAMAZEPINE

Pharmtech & Ingredients
Not Confirmed
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Brand Name : CARBAMAZEPINE

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Pharmtech & Ingredients
Not Confirmed

Unique Biotech Limited

Dosage Form : TABLET, EXTENDED RELEASE...

Brand Name : CARBAMAZEPINE

Dosage Strength : 200MG

Packaging :

Approval Date : 2020-04-24

Application Number : 211623

Regulatory Info : RX

Registration Country : USA

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06

Brand Name : CARBAMAZEPINE

Pharmtech & Ingredients
Not Confirmed
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Brand Name : CARBAMAZEPINE

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Pharmtech & Ingredients
Not Confirmed

Unique Biotech Limited

Dosage Form : TABLET, EXTENDED RELEASE...

Brand Name : CARBAMAZEPINE

Dosage Strength : 400MG

Packaging :

Approval Date : 2020-04-24

Application Number : 211623

Regulatory Info : RX

Registration Country : USA

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07

Brand Name : CETIRIZINE HYDROCHLO...

Pharmtech & Ingredients
Not Confirmed
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Brand Name : CETIRIZINE HYDROCHLO...

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Pharmtech & Ingredients
Not Confirmed

Unique Biotech Limited

Dosage Form : TABLET;ORAL

Brand Name : CETIRIZINE HYDROCHLORIDE ...

Dosage Strength : 5MG

Packaging :

Approval Date : 2009-08-26

Application Number : 77829

Regulatory Info : OTC

Registration Country : USA

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08

Brand Name : CETIRIZINE HYDROCHLO...

Pharmtech & Ingredients
Not Confirmed
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Brand Name : CETIRIZINE HYDROCHLO...

arrow
Pharmtech & Ingredients
Not Confirmed

Unique Biotech Limited

Dosage Form : TABLET;ORAL

Brand Name : CETIRIZINE HYDROCHLORIDE ...

Dosage Strength : 10MG

Packaging :

Approval Date : 2009-08-26

Application Number : 77829

Regulatory Info : OTC

Registration Country : USA

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09

Brand Name : CETIRIZINE HYDROCHLO...

Pharmtech & Ingredients
Not Confirmed
arrow

Brand Name : CETIRIZINE HYDROCHLO...

arrow
Pharmtech & Ingredients
Not Confirmed

Unique Biotech Limited

Dosage Form : TABLET;ORAL

Brand Name : CETIRIZINE HYDROCHLORIDE ...

Dosage Strength : 5MG

Packaging :

Approval Date : 2009-08-26

Application Number : 77829

Regulatory Info : OTC

Registration Country : USA

blank

10

Brand Name : CETIRIZINE HYDROCHLO...

Pharmtech & Ingredients
Not Confirmed
arrow

Brand Name : CETIRIZINE HYDROCHLO...

arrow
Pharmtech & Ingredients
Not Confirmed

Unique Biotech Limited

Dosage Form : TABLET;ORAL

Brand Name : CETIRIZINE HYDROCHLORIDE ...

Dosage Strength : 10MG

Packaging :

Approval Date : 2009-08-26

Application Number : 77829

Regulatory Info : OTC

Registration Country : USA

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