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01 5ADAPALENE

02 2ADAPALENE; BENZOYL PEROXIDE

03 1AMOROLFINE HYDROCHLORIDE

04 4Adapalene

05 2Amorolfine

06 1Amorolfine HCl

07 3Amorolfine Hydrochloride

08 1BENZOYL PEROXIDE

09 1BENZOYL PEROXIDE; TRETINOIN

10 1BRIMONIDINE TARTRATE

11 1Benzoyl Peroxide

12 1Benzoyl peroxide

13 1CALCITRIOL

14 3CLOBETASOL PROPIONATE

15 1Clobetasol Propiomate

16 1Clobetasol propionate

17 3DESONIDE

18 1DOXYCYCLINE

19 1DOXYCYCLINE HYCLATE

20 1FLUOCINOLONE ACETONIDE

21 1FLUOCINOLONE ACETONIDE; HYDROQUINONE; TRETINOIN

22 1IVERMECTIN

23 1Ivermectin

24 2Lymecycline

25 1METHYL AMINOLEVULINATE HYDROCHLORIDE

26 4METRONIDAZOLE

27 1Methyl Aminolevulinate

28 1Metronidazole

29 2NEMOLIZUMAB-ILTO

30 2TRIFAROTENE

31 1Tretinoin

32 1amorolfinhydroklorid

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PharmaCompass

01

Brand Name : DIFFERIN

Plastics Recycling EU
Not Confirmed
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Brand Name : DIFFERIN

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Plastics Recycling EU
Not Confirmed

GALDERMA LABS LP

Dosage Form : SOLUTION;TOPICAL

Brand Name : DIFFERIN

Dosage Strength : 0.1% **Federal Registe...

Packaging :

Approval Date : 1996-05-31

Application Number : 20338

Regulatory Info : DISCN

Registration Country : USA

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02

Brand Name : DIFFERIN

Plastics Recycling EU
Not Confirmed
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Brand Name : DIFFERIN

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Plastics Recycling EU
Not Confirmed

GALDERMA LABS LP

Dosage Form : GEL;TOPICAL

Brand Name : DIFFERIN

Dosage Strength : 0.1%

Packaging :

Approval Date : 2016-07-08

Application Number : 20380

Regulatory Info : OTC

Registration Country : USA

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03

Brand Name : DIFFERIN

Plastics Recycling EU
Not Confirmed
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Brand Name : DIFFERIN

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Plastics Recycling EU
Not Confirmed

GALDERMA LABS LP

Dosage Form : CREAM;TOPICAL

Brand Name : DIFFERIN

Dosage Strength : 0.1%

Packaging :

Approval Date : 2000-05-26

Application Number : 20748

Regulatory Info : RX

Registration Country : USA

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04

Brand Name : DIFFERIN

Plastics Recycling EU
Not Confirmed
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Brand Name : DIFFERIN

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Plastics Recycling EU
Not Confirmed

GALDERMA LABS LP

Dosage Form : GEL;TOPICAL

Brand Name : DIFFERIN

Dosage Strength : 0.3%

Packaging :

Approval Date : 2007-06-19

Application Number : 21753

Regulatory Info : RX

Registration Country : USA

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05

Brand Name : DIFFERIN

Plastics Recycling EU
Not Confirmed
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Brand Name : DIFFERIN

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Plastics Recycling EU
Not Confirmed

GALDERMA LABS LP

Dosage Form : LOTION;TOPICAL

Brand Name : DIFFERIN

Dosage Strength : 0.1%

Packaging :

Approval Date : 2010-03-17

Application Number : 22502

Regulatory Info : DISCN

Registration Country : USA

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06

Brand Name : Epiduo 0,1 % / 2,5 %

Plastics Recycling EU
Not Confirmed
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Brand Name : Epiduo 0,1 % / 2,5 %

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Plastics Recycling EU
Not Confirmed

GALDERMA LABS LP

Dosage Form : Gel

Brand Name : Epiduo 0,1 % / 2,5 %

Dosage Strength : 1mg/g

Packaging : 30X1mg/g

Approval Date :

Application Number :

Regulatory Info : Originator

Registration Country : South Africa

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07

Brand Name : Differin Gel

Plastics Recycling EU
Not Confirmed
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Brand Name : Differin Gel

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Plastics Recycling EU
Not Confirmed

GALDERMA LABS LP

Dosage Form : Gel

Brand Name : Differin Gel

Dosage Strength : 1mg/g

Packaging : 30X1mg/g

Approval Date :

Application Number :

Regulatory Info : Originator

Registration Country : South Africa

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08

Brand Name : Differin Cream

Plastics Recycling EU
Not Confirmed
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Brand Name : Differin Cream

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Plastics Recycling EU
Not Confirmed

GALDERMA LABS LP

Dosage Form : CRM

Brand Name : Differin Cream

Dosage Strength : 1mg/g

Packaging : 30X1mg/g

Approval Date :

Application Number :

Regulatory Info : Originator

Registration Country : South Africa

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09

Brand Name : Epiduo Forte

Plastics Recycling EU
Not Confirmed
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Brand Name : Epiduo Forte

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Plastics Recycling EU
Not Confirmed

GALDERMA LABS LP

Dosage Form : Gel

Brand Name : Epiduo Forte

Dosage Strength : 3mg/g

Packaging : 30X1mg/g

Approval Date :

Application Number :

Regulatory Info : Originator

Registration Country : South Africa

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10

Brand Name : EPIDUO

Plastics Recycling EU
Not Confirmed
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Brand Name : EPIDUO

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Plastics Recycling EU
Not Confirmed

GALDERMA LABS LP

Dosage Form : GEL;TOPICAL

Brand Name : EPIDUO

Dosage Strength : 0.1%;2.5%

Packaging :

Approval Date : 2008-12-08

Application Number : 22320

Regulatory Info : RX

Registration Country : USA

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