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
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
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20 1EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
21 1EQ 120MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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25 1EQ 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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
01 13DISCN
02 15RX
03 1Blank
RLD : Yes
TE Code :
Dosage Form : AEROSOL, FOAM; TOPICAL
Proprietary Name : SORILUX
Dosage Strength : 0.005%
Approval Date : 2010-10-06
Application Number : 22563
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : No
TE Code :
CHLORPHENIRAMINE MALEATE; HYDROCODONE BITARTRATE; PSEUDOEPHEDRINE HYDROCHLORIDE
Dosage Form : SOLUTION; ORAL
Proprietary Name : HYDROCODONE BITARTRATE, ...
Dosage Strength : 4MG/5ML;5MG/5ML;60MG/5ML
Approval Date : 2015-08-03
Application Number : 205657
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Dosage Form : CAPSULE, DELAYED RELEASE; ORAL
Proprietary Name : DORYX
Dosage Strength : EQ 100MG BASE
Approval Date : 1985-07-22
Application Number : 50582
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : CAPSULE, DELAYED RELEASE; ORAL
Proprietary Name : DORYX
Dosage Strength : EQ 75MG BASE
Approval Date : 2001-08-13
Application Number : 50582
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET, DELAYED RELEASE; ORAL
Proprietary Name : DORYX
Dosage Strength : EQ 75MG BASE
Approval Date : 2005-05-06
Application Number : 50795
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET, DELAYED RELEASE; ORAL
Proprietary Name : DORYX
Dosage Strength : EQ 100MG BASE **Federal ...
Approval Date : 2005-05-06
Application Number : 50795
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET, DELAYED RELEASE; ORAL
Proprietary Name : DORYX
Dosage Strength : EQ 150MG BASE
Approval Date : 2008-06-20
Application Number : 50795
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET, DELAYED RELEASE; ORAL
Proprietary Name : DORYX
Dosage Strength : EQ 80MG BASE
Approval Date : 2013-04-11
Application Number : 50795
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB
Dosage Form : TABLET, DELAYED RELEASE; ORAL
Proprietary Name : DORYX
Dosage Strength : EQ 200MG BASE
Approval Date : 2013-04-11
Application Number : 50795
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
Dosage Form : TABLET, DELAYED RELEASE; ORAL
Proprietary Name : DORYX
Dosage Strength : EQ 50MG BASE **Federal R...
Approval Date : 2014-12-19
Application Number : 50795
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
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