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
01 2GALDERMA LABS
02 34GALDERMA LABS LP
03 17Galderma Laboratories South Africa (Pty) Ltd
01 2CAP
02 1CAPSULE;ORAL
03 1CRE
04 9CREAM;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06 10.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 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 130mg
23 13MCG/GM
24 13mg/g
25 140MG
26 25%
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34 1EQ 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 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 : 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
