01 2ALOSETRON HYDROCHLORIDE
02 2ATROPINE SULFATE; DIFENOXIN HYDROCHLORIDE
03 1AURANOFIN
04 2AZATHIOPRINE
05 2HYDROCORTISONE ACETATE
06 4HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE
07 1ITRACONAZOLE
08 1LABETALOL HYDROCHLORIDE
09 4NAFTIFINE HYDROCHLORIDE
10 5PAROXETINE MESYLATE
01 2CAPSULE;ORAL
02 6CREAM;TOPICAL
03 2GEL;TOPICAL
04 1INJECTABLE;INJECTION
05 2LOTION;TOPICAL
06 11TABLET;ORAL
01 10.025MG;0.5MG
02 10.025MG;1MG
03 10.5%;1%
04 11%
05 11% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
06 21%;1%
07 32%
08 12.5%
09 12.5%;1%
10 1200MG
11 125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
12 13MG
13 150MG
14 15MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
15 1EQ 0.5MG BASE
16 1EQ 10MG BASE
17 1EQ 1MG BASE
18 1EQ 20MG BASE
19 1EQ 30MG BASE
20 1EQ 40MG BASE
21 1EQ 7.5MG BASE
01 10DISCN
02 14RX
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : LOTRONEX
Dosage Strength : EQ 1MG BASE
Approval Date : 2000-02-09
Application Number : 21107
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : LOTRONEX
Dosage Strength : EQ 0.5MG BASE
Approval Date : 2003-12-23
Application Number : 21107
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : No
TE Code :
ATROPINE SULFATE; DIFENOXIN HYDROCHLORIDE
Dosage Form : TABLET; ORAL
Proprietary Name : MOTOFEN HALF-STRENGTH
Dosage Strength : 0.025MG;0.5MG
Approval Date : 1982-01-01
Application Number : 17744
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
ATROPINE SULFATE; DIFENOXIN HYDROCHLORIDE
Dosage Form : TABLET; ORAL
Proprietary Name : MOTOFEN
Dosage Strength : 0.025MG;1MG
Approval Date : 1982-01-01
Application Number : 17744
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : RIDAURA
Dosage Strength : 3MG
Approval Date : 1985-05-24
Application Number : 18689
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : IMURAN
Dosage Strength : 50MG
Approval Date : 1982-01-01
Application Number : 16324
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : IMURAN
Dosage Strength : 25MG **Federal Register ...
Approval Date : 1982-01-01
Application Number : 16324
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Dosage Form : CREAM; TOPICAL
Proprietary Name : MICORT-HC
Dosage Strength : 2.5%
Approval Date : 2001-02-27
Application Number : 40396
RX/OTC/DISCN : RX
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : CREAM; TOPICAL
Proprietary Name : MICORT-HC
Dosage Strength : 2%
Approval Date : 2002-03-29
Application Number : 40398
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE
Dosage Form : CREAM; TOPICAL
Proprietary Name : PRAMOSONE
Dosage Strength : 1%;1%
Approval Date : 1982-01-01
Application Number : 85368
RX/OTC/DISCN : RX
RLD : No
TE Code :
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