01 5ADAPALENE
02 2ADAPALENE; BENZOYL PEROXIDE
03 1AMOROLFINE HYDROCHLORIDE
04 4Adapalene
05 2Amorolfine
06 1Amorolfine HCl
07 3Amorolfine Hydrochloride
08 1BRIMONIDINE TARTRATE
09 1Benzoyl Peroxide
10 1Benzoyl peroxide
11 1CALCITRIOL
12 3CLOBETASOL PROPIONATE
13 1Clobetasol Propiomate
14 1Clobetasol propionate
15 3DESONIDE
16 1DOXYCYCLINE
17 1DOXYCYCLINE HYCLATE
18 1FLUOCINOLONE ACETONIDE
19 1FLUOCINOLONE ACETONIDE; HYDROQUINONE; TRETINOIN
20 1IVERMECTIN
21 1Ivermectin
22 2Lymecycline
23 1METHYL AMINOLEVULINATE HYDROCHLORIDE
24 4METRONIDAZOLE
25 1Methyl Aminolevulinate
26 1Metronidazole
27 2NEMOLIZUMAB-ILTO
28 2TRIFAROTENE
29 1Tretinoin
30 1amorolfinhydroklorid
01 2GALDERMA LABS
02 32GALDERMA LABS LP
03 17Galderma Laboratories South Africa (Pty) Ltd
01 2CAP
02 1CAPSULE;ORAL
03 1CRE
04 7CREAM;TOPICAL
05 4CRM
06 1Crème
07 7GEL;TOPICAL
08 7Gel
09 2INJECTABLE;INJECTION
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06 10.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 30.75%
13 10.75% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
14 21%
15 110mg/g
16 1150mg
17 1160mg/g
18 31mg/g
19 225mg/g
20 1300mg
21 130MG
22 130mg
23 13MCG/GM
24 13mg/g
25 140MG
26 15%
27 15% w/v
28 150 µg/g
29 1500µg/g
30 250mg/ml
31 1Cream Derm 20 G 0.25%
32 1EQ 0.33% BASE
33 1EQ 16.8% BASE
34 1EQ 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
35 1Enamel Nails 1 Bottle 2.5 Ml 5%
36 1Loceryl Nagellack, Lös 5 %, 5 ml
37 1Loceryl, Creme 0.250 %, 20 g
01 17South Africa
02 1Sweden
03 5U.S.A
04 28USA
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
Dosage Strength : 0.1%;2.5%
Packaging :
Approval Date : 2008-12-08
Application Number : 22320
Regulatory Info : RX
Registration Country : USA
