01 2ALOSETRON HYDROCHLORIDE
02 2ATROPINE SULFATE; DIFENOXIN HYDROCHLORIDE
03 1AURANOFIN
04 2AZATHIOPRINE
05 1CLOCORTOLONE PIVALATE
06 1CROTAMITON
07 1HYDROCORTISONE
08 2HYDROCORTISONE ACETATE
09 4HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE
10 4NAFTIFINE HYDROCHLORIDE
11 1PAROXETINE MESYLATE
12 4PIRFENIDONE
13 11SOTALOL HYDROCHLORIDE
14 5TIZANIDINE HYDROCHLORIDE
01 6CAPSULE;ORAL
02 7CREAM;TOPICAL
03 2GEL;TOPICAL
04 4LOTION;TOPICAL
05 22TABLET;ORAL
01 10.025MG;0.5MG
02 10.025MG;1MG
03 10.1%
04 10.5%;1%
05 11%
06 11% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
07 21%;1%
08 110%
09 1100MG
10 2120MG
11 2160MG
12 42%
13 12.5%
14 12.5%;1%
15 1240MG
16 125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
17 2267MG
18 1320MG
19 13MG
20 140MG
21 150MG
22 1534MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
23 160MG
24 1801MG
25 280MG
26 1EQ 0.5MG BASE
27 1EQ 1MG BASE
28 1EQ 2MG BASE
29 1EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
30 2EQ 4MG BASE
31 1EQ 6MG BASE
32 1EQ 7.5MG BASE
01 10DISCN
02 31RX
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 : Yes
TE Code : AB
Dosage Form : CREAM; TOPICAL
Proprietary Name : CLODERM
Dosage Strength : 0.1%
Approval Date : 1982-01-01
Application Number : 17765
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : No
TE Code : AT
Dosage Form : LOTION; TOPICAL
Proprietary Name : CROTAN
Dosage Strength : 10%
Approval Date : 1982-01-01
Application Number : 87204
RX/OTC/DISCN : RX
RLD : No
TE Code : AT
RLD : Yes
TE Code :
Dosage Form : LOTION; TOPICAL
Proprietary Name : ALA-SCALP
Dosage Strength : 2%
Approval Date : 1982-01-01
Application Number : 83231
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
