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 1NEMOLIZUMAB-ILTO
30 1TRIFAROTENE
31 1Tretinoin
32 1amorolfinhydroklorid
01 2GALDERMA LABS
02 33GALDERMA LABS LP
03 16Galderma Laboratories South Africa (Pty) Ltd
01 2CAP
02 1CAPSULE;ORAL
03 9CREAM;TOPICAL
04 4CRM
05 1Crème
06 7GEL;TOPICAL
07 7Gel
08 1INJECTABLE;INJECTION
09 4LOTION;TOPICAL
10 1MEDICAL NAIL POLISH
11 1Medical nail polish
12 2OINTMENT;TOPICAL
13 2PAI
14 1SHA
15 2SHAMPOO;TOPICAL
16 1SOL
17 1SOLUTION;TOPICAL
18 1SPRAY;TOPICAL
19 1TABLET;ORAL
20 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06 10.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 225mg/g
19 13%;0.1%
20 1300mg
21 130MG
22 13MCG/GM
23 13mg/g
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32 1EQ 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 16South Africa
02 1Sweden
03 5U.S.A
04 29USA
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 : Gel
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 : Originator
Registration Country : South Africa
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
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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