01 1CALCIPOTRIENE
02 1CHLORPHENIRAMINE MALEATE; HYDROCODONE BITARTRATE; PSEUDOEPHEDRINE HYDROCHLORIDE
03 10DOXYCYCLINE HYCLATE
04 1DROSPIRENONE; ESTETROL
05 2ESTRADIOL
06 2ESTRADIOL; PROGESTERONE
07 1ETHINYL ESTRADIOL; LEVONORGESTREL
08 1ETHINYL ESTRADIOL; SEGESTERONE ACETATE
09 4FENTANYL
10 1HALOBETASOL PROPIONATE
11 1HYDROCODONE BITARTRATE; PSEUDOEPHEDRINE HYDROCHLORIDE
12 1ITRACONAZOLE
13 1OXYMETAZOLINE HYDROCHLORIDE
14 1TAMOXIFEN CITRATE
15 1TAZAROTENE
16 6doxycycline
17 3erythromycin
01 25MAYNE PHARMA
02 1MAYNE PHARMA COMMRCL
03 3MAYNE PHARMA INC
04 9Mayne Products Pty Ltd
01 3AEROSOL, FOAM;TOPICAL
02 2CAPSULE, DELAYED RELEASE;ORAL
03 3CAPSULE;ORAL
04 1CREAM;TOPICAL
05 4FILM, EXTENDED RELEASE;TRANSDERMAL
06 2INSERT;VAGINAL
07 1RING;VAGINAL
08 3SOLUTION;ORAL
09 8TABLET, DELAYED RELEASE;ORAL
10 2TABLET;ORAL
11 9Blank
01 10.004MG
02 10.005%
03 10.013MG/24HR;0.15MG/24HR
04 10.01MG
05 10.02MG,0.15MG;0.025MG,0.15MG;0.03MG,0.15MG;0.01MG,N/A
06 10.05%
07 10.1%
08 10.5MG;100MG
09 11%
10 1100MCG/HR
11 11MG;100MG
12 125MCG/HR
13 13MG;14.2MG
14 14MG/5ML;5MG/5ML;60MG/5ML
15 150MCG/HR
16 15MG/5ML;60MG/5ML
17 165MG
18 175MCG/HR
19 1EQ 100MG BASE
20 1EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
21 1EQ 120MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
22 1EQ 150MG BASE
23 1EQ 200MG BASE
24 1EQ 20MG BASE/10ML
25 1EQ 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
26 1EQ 60MG BASE
27 2EQ 75MG BASE
28 1EQ 80MG BASE
29 9Blank
01 9Australia
02 29USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : AEROSOL, FOAM;TOPICAL
Brand Name : SORILUX
Dosage Strength : 0.005%
Packaging :
Approval Date : 2010-10-06
Application Number : 22563
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
CHLORPHENIRAMINE MALEATE; HYDROCODONE BITARTRATE; PSEUDOEPHEDRINE HYDROCHLORIDE
Dosage Form : SOLUTION;ORAL
Brand Name : HYDROCODONE BITARTRATE, C...
Dosage Strength : 4MG/5ML;5MG/5ML;60MG/5...
Packaging :
Approval Date : 2015-08-03
Application Number : 205657
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : Australia
Dosage Form :
Brand Name : Mayne Pharma Doxycycline
Dosage Strength :
Packaging : 7
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Dosage Form :
Brand Name : Mayne Pharma Doxycycline
Dosage Strength :
Packaging : 7
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Dosage Form :
Brand Name : Mayne Pharma Doxycycline
Dosage Strength :
Packaging : 25
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Dosage Form :
Brand Name : Mayne Pharma Doxycycline
Dosage Strength :
Packaging : 7
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Dosage Form :
Brand Name : Mayne Pharma Doxycycline
Dosage Strength :
Packaging : 21
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Dosage Form :
Brand Name : Mayne Pharma Doxycycline
Dosage Strength :
Packaging : 7
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : CAPSULE, DELAYED RELEASE...
Brand Name : DORYX
Dosage Strength : EQ 75MG BASE
Packaging :
Approval Date : 2001-08-13
Application Number : 50582
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET, DELAYED RELEASE;...
Brand Name : DORYX
Dosage Strength : EQ 200MG BASE
Packaging :
Approval Date : 2013-04-11
Application Number : 50795
Regulatory Info : RX
Registration Country : USA
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