Please Wait
Applying Filters...
Menu
Xls
Filters Filter
Cross PopUp
FILTER :

filter clear-filterReset all filters

01 1ADAPALENE

02 1CLOTRIMAZOLE

03 1DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM

04 1DOCOSANOL

05 1ESOMEPRAZOLE MAGNESIUM

06 1FAMOTIDINE

07 3FEXOFENADINE HYDROCHLORIDE

08 1IBUPROFEN

09 1LORATADINE; PSEUDOEPHEDRINE SULFATE

10 1MICONAZOLE NITRATE

11 4MINOXIDIL

12 30NICOTINE POLACRILEX

13 1OMEPRAZOLE MAGNESIUM

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

PharmaCompass

01

Brand Name : ADAPALENE

Antibody Engineering
Not Confirmed
arrow

Brand Name : ADAPALENE

arrow
Antibody Engineering
Not Confirmed

PL Developments

Dosage Form : GEL;TOPICAL

Brand Name : ADAPALENE

Dosage Strength : 0.1%

Packaging :

Approval Date : 2010-06-02

Application Number : 90962

Regulatory Info : OTC

Registration Country : USA

blank

02

Brand Name : CLOTRIMAZOLE

Antibody Engineering
Not Confirmed
arrow

Brand Name : CLOTRIMAZOLE

arrow
Antibody Engineering
Not Confirmed

PL Developments

Dosage Form : CREAM;VAGINAL

Brand Name : CLOTRIMAZOLE

Dosage Strength : 1%

Packaging :

Approval Date : 1993-07-16

Application Number : 74165

Regulatory Info : OTC

Registration Country : USA

blank

03

Brand Name : NAPROXEN SODIUM AND ...

Antibody Engineering
Not Confirmed
arrow

Brand Name : NAPROXEN SODIUM AND ...

arrow
Antibody Engineering
Not Confirmed

PL Developments

Dosage Form : TABLET;ORAL

Brand Name : NAPROXEN SODIUM AND DIPHE...

Dosage Strength : 25MG;220MG

Packaging :

Approval Date : 2019-01-25

Application Number : 207597

Regulatory Info : DISCN

Registration Country : USA

blank

04

Brand Name : DOCOSANOL

Antibody Engineering
Not Confirmed
arrow

Brand Name : DOCOSANOL

arrow
Antibody Engineering
Not Confirmed

PL Developments

Dosage Form : CREAM;TOPICAL

Brand Name : DOCOSANOL

Dosage Strength : 10%

Packaging :

Approval Date : 2018-11-19

Application Number : 208754

Regulatory Info : OTC

Registration Country : USA

blank

05

Brand Name : ESOMEPRAZOLE MAGNESI...

Antibody Engineering
Not Confirmed
arrow

Brand Name : ESOMEPRAZOLE MAGNESI...

arrow
Antibody Engineering
Not Confirmed

PL Developments

Dosage Form : TABLET, DELAYED RELEASE;...

Brand Name : ESOMEPRAZOLE MAGNESIUM

Dosage Strength : EQ 20MG BASE

Packaging :

Approval Date : 2019-03-05

Application Number : 209202

Regulatory Info : DISCN

Registration Country : USA

blank

06

Brand Name : FAMOTIDINE

Antibody Engineering
Not Confirmed
arrow

Brand Name : FAMOTIDINE

arrow
Antibody Engineering
Not Confirmed

PL Developments

Dosage Form : TABLET;ORAL

Brand Name : FAMOTIDINE

Dosage Strength : 10MG

Packaging :

Approval Date : 2001-07-26

Application Number : 75512

Regulatory Info : OTC

Registration Country : USA

blank

07

Brand Name : FEXOFENADINE HYDROCH...

Antibody Engineering
Not Confirmed
arrow

Brand Name : FEXOFENADINE HYDROCH...

arrow
Antibody Engineering
Not Confirmed

PL Developments

Dosage Form : SUSPENSION;ORAL

Brand Name : FEXOFENADINE HYDROCHLORID...

Dosage Strength : 30MG/5ML

Packaging :

Approval Date : 2012-07-25

Application Number : 201311

Regulatory Info : DISCN

Registration Country : USA

blank

08

Brand Name : CHILDRENS FEXOFENADI...

Antibody Engineering
Not Confirmed
arrow

Brand Name : CHILDRENS FEXOFENADI...

arrow
Antibody Engineering
Not Confirmed

PL Developments

Dosage Form : SUSPENSION;ORAL

Brand Name : CHILDRENS FEXOFENADINE HY...

Dosage Strength : 30MG/5ML

Packaging :

Approval Date : 2014-11-18

Application Number : 203330

Regulatory Info : OTC

Registration Country : USA

blank

09

Brand Name : CHILDRENS FEXOFENADI...

Antibody Engineering
Not Confirmed
arrow

Brand Name : CHILDRENS FEXOFENADI...

arrow
Antibody Engineering
Not Confirmed

PL Developments

Dosage Form : SUSPENSION;ORAL

Brand Name : CHILDRENS FEXOFENADINE HY...

Dosage Strength : 30MG/5ML

Packaging :

Approval Date : 2014-11-18

Application Number : 203330

Regulatory Info : OTC

Registration Country : USA

blank

10

Brand Name : IBUPROFEN

Antibody Engineering
Not Confirmed
arrow

Brand Name : IBUPROFEN

arrow
Antibody Engineering
Not Confirmed

PL Developments

Dosage Form : SUSPENSION;ORAL

Brand Name : IBUPROFEN

Dosage Strength : 100MG/5ML

Packaging :

Approval Date : 1999-04-30

Application Number : 74916

Regulatory Info : OTC

Registration Country : USA

blank