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01 2CETIRIZINE HYDROCHLORIDE

02 1CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE

03 1CLEMASTINE FUMARATE

04 1DIPHENHYDRAMINE CITRATE; IBUPROFEN

05 1FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE

06 1LORATADINE

07 1NAPROXEN SODIUM

08 2NICOTINE POLACRILEX

09 2ZOLMITRIPTAN

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PharmaCompass

01

Brand Name : CETIRIZINE HYDROCHLO...

U.S.A
Pharmtech & Ingredients
Not Confirmed
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Brand Name : CETIRIZINE HYDROCHLO...

U.S.A
Pharmtech & Ingredients
Not Confirmed
arrow

PLD ACQUISITIONS

Dosage Form : TABLET; ORAL

Proprietary Name : CETIRIZINE HYDROCHLORIDE...

Dosage Strength : 5MG

Approval Date : 2007-12-27

Application Number : 77946

RX/OTC/DISCN : OTC

RLD : No

TE Code :

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02

Brand Name : CETIRIZINE HYDROCHLO...

U.S.A
Pharmtech & Ingredients
Not Confirmed
arrow

Brand Name : CETIRIZINE HYDROCHLO...

U.S.A
Pharmtech & Ingredients
Not Confirmed
arrow

PLD ACQUISITIONS

Dosage Form : TABLET; ORAL

Proprietary Name : CETIRIZINE HYDROCHLORIDE...

Dosage Strength : 10MG

Approval Date : 2007-12-27

Application Number : 77946

RX/OTC/DISCN : OTC

RLD : No

TE Code :

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03

Brand Name : CETIRIZINE HYDROCHLO...

U.S.A
Pharmtech & Ingredients
Not Confirmed
arrow

Brand Name : CETIRIZINE HYDROCHLO...

U.S.A
Pharmtech & Ingredients
Not Confirmed
arrow

PLD ACQUISITIONS

Dosage Form : TABLET, EXTENDED RELEASE; ORAL

Proprietary Name : CETIRIZINE HYDROCHLORIDE...

Dosage Strength : 5MG;120MG

Approval Date : 2008-03-05

Application Number : 77991

RX/OTC/DISCN : OTC

RLD : No

TE Code :

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04

Brand Name : CLEMASTINE FUMARATE

U.S.A
Pharmtech & Ingredients
Not Confirmed
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Brand Name : CLEMASTINE FUMARATE

U.S.A
Pharmtech & Ingredients
Not Confirmed
arrow

PLD ACQUISITIONS

Dosage Form : TABLET; ORAL

Proprietary Name : CLEMASTINE FUMARATE

Dosage Strength : 1.34MG

Approval Date : 1993-10-31

Application Number : 73458

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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05

Brand Name : IBUPROFEN AND DIPHEN...

U.S.A
Pharmtech & Ingredients
Not Confirmed
arrow

Brand Name : IBUPROFEN AND DIPHEN...

U.S.A
Pharmtech & Ingredients
Not Confirmed
arrow

PLD ACQUISITIONS

Dosage Form : TABLET; ORAL

Proprietary Name : IBUPROFEN AND DIPHENHYDR...

Dosage Strength : 38MG;200MG

Approval Date : 2024-04-11

Application Number : 211404

RX/OTC/DISCN : OTC

RLD : No

TE Code :

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06

Brand Name : FEXOFENADINE HYDROCH...

U.S.A
Pharmtech & Ingredients
Not Confirmed
arrow

Brand Name : FEXOFENADINE HYDROCH...

U.S.A
Pharmtech & Ingredients
Not Confirmed
arrow

PLD ACQUISITIONS

Dosage Form : TABLET, EXTENDED RELEASE; ORA...

Proprietary Name : FEXOFENADINE HYDROCHLORI...

Dosage Strength : 60MG; 120MG

Approval Date :

Application Number : 77999

RX/OTC/DISCN :

RLD :

TE Code :

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07

Brand Name : LORATADINE

U.S.A
Pharmtech & Ingredients
Not Confirmed
arrow

Brand Name : LORATADINE

U.S.A
Pharmtech & Ingredients
Not Confirmed
arrow

PLD ACQUISITIONS

Dosage Form : TABLET; ORAL

Proprietary Name : LORATADINE

Dosage Strength : 10MG

Approval Date : 2003-01-21

Application Number : 75209

RX/OTC/DISCN : OTC

RLD : No

TE Code :

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08

Brand Name : NAPROXEN SODIUM

U.S.A
Pharmtech & Ingredients
Not Confirmed
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Brand Name : NAPROXEN SODIUM

U.S.A
Pharmtech & Ingredients
Not Confirmed
arrow

PLD ACQUISITIONS

Dosage Form : TABLET; ORAL

Proprietary Name : NAPROXEN SODIUM

Dosage Strength : 220MG

Approval Date : 1997-01-13

Application Number : 74646

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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09

Brand Name : NICOTINE POLACRILEX

U.S.A
Pharmtech & Ingredients
Not Confirmed
arrow

Brand Name : NICOTINE POLACRILEX

U.S.A
Pharmtech & Ingredients
Not Confirmed
arrow

PLD ACQUISITIONS

Dosage Form : TROCHE/LOZENGE; ORAL

Proprietary Name : NICOTINE POLACRILEX

Dosage Strength : EQ 2MG BASE

Approval Date : 2019-02-07

Application Number : 207868

RX/OTC/DISCN : OTC

RLD : No

TE Code :

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10

Brand Name : NICOTINE POLACRILEX

U.S.A
Pharmtech & Ingredients
Not Confirmed
arrow

Brand Name : NICOTINE POLACRILEX

U.S.A
Pharmtech & Ingredients
Not Confirmed
arrow

PLD ACQUISITIONS

Dosage Form : TROCHE/LOZENGE; ORAL

Proprietary Name : NICOTINE POLACRILEX

Dosage Strength : EQ 4MG BASE

Approval Date : 2019-02-07

Application Number : 207868

RX/OTC/DISCN : OTC

RLD : No

TE Code :

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