01 5ADAPALENE
02 2ADAPALENE; BENZOYL PEROXIDE
03 1AMOROLFINE HYDROCHLORIDE
04 3Adapalene
05 2Amorolfine
06 1Amorolfine HCl
07 3Amorolfine Hydrochloride
08 1BENZOYL PEROXIDE
09 1BENZOYL PEROXIDE; TRETINOIN
10 1BRIMONIDINE TARTRATE
11 1Benzoyl peroxide
12 1CALCITRIOL
13 3CLOBETASOL PROPIONATE
14 1Clobetasol Propiomate
15 1Clobetasol propionate
16 3DESONIDE
17 1DOXYCYCLINE
18 1DOXYCYCLINE HYCLATE
19 1FLUOCINOLONE ACETONIDE
20 1FLUOCINOLONE ACETONIDE; HYDROQUINONE; TRETINOIN
21 1IVERMECTIN
22 1Ivermectin
23 2Lymecycline
24 1METHYL AMINOLEVULINATE HYDROCHLORIDE
25 4METRONIDAZOLE
26 1Methyl Aminolevulinate
27 1Metronidazole
28 2NEMOLIZUMAB-ILTO
29 1TRIFAROTENE
30 1Tretinoin
31 1amorolfinhydroklorid
01 2GALDERMA LABS
02 34GALDERMA LABS LP
03 14Galderma Laboratories South Africa (Pty) Ltd
01 2CAP
02 1CAPSULE;ORAL
03 9CREAM;TOPICAL
04 4CRM
05 1Crème
06 7GEL;TOPICAL
07 3Gel
08 2INJECTABLE;INJECTION
09 2JEL
10 4LOTION;TOPICAL
11 1MEDICAL NAIL POLISH
12 1Medical nail polish
13 2OINTMENT;TOPICAL
14 2PAI
15 1SHA
16 2SHAMPOO;TOPICAL
17 1SOL
18 1SOLUTION;TOPICAL
19 1SPRAY;TOPICAL
20 1TABLET;ORAL
21 2Blank
01 10.005%
02 10.01%
03 10.01%;4%;0.05%
04 60.05%
05 30.1%
06 10.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
07 10.1%;2.5%
08 10.3%
09 10.3%;2.5%
10 10.5mg
11 10.5mg/g
12 40.75%
13 21%
14 110mg/g
15 1150mg
16 1160mg/g
17 31mg/g
18 125mg/g
19 13%;0.1%
20 1300mg
21 130MG
22 130mg
23 13MCG/GM
24 140MG
25 25%
26 15% w/v
27 1500µg/g
28 250mg/ml
29 1Cream Derm 20 G 0.25%
30 1EQ 0.33% BASE
31 1EQ 16.8% BASE
32 1EQ 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
33 1Enamel Nails 1 Bottle 2.5 Ml 5%
34 1Loceryl Nagellack, Lös 5 %, 5 ml
35 1Loceryl, Creme 0.250 %, 20 g
01 14South Africa
02 1Sweden
03 5U.S.A
04 30USA
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : OTC
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : Originator
Registration Country : South Africa
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
Regulatory Info : Originator
Registration Country : South Africa
Dosage Form : JEL
Brand Name : Differin Gel
Dosage Strength : 1mg/g
Packaging : 30X1mg/g
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
Dosage Form : GEL;TOPICAL
Brand Name : EPIDUO FORTE
Dosage Strength : 0.3%;2.5%
Packaging :
Approval Date : 2015-07-15
Application Number : 207917
Regulatory Info : RX
Registration Country : USA
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