01 1ALFUZOSIN HYDROCHLORIDE
02 1ALITRETINOIN
03 6DIGOXIN
04 1HYDROXYCHLOROQUINE SULFATE
05 2NILUTAMIDE
06 1PHENOXYBENZAMINE HYDROCHLORIDE
07 2PILOCARPINE HYDROCHLORIDE
08 3PREDNISOLONE SODIUM PHOSPHATE
09 1TRANYLCYPROMINE SULFATE
10 2TRIAMTERENE
11 3ZONISAMIDE
01 6CAPSULE;ORAL
02 1GEL;TOPICAL
03 1TABLET, EXTENDED RELEASE;ORAL
04 3TABLET, ORALLY DISINTEGRATING;ORAL
05 12TABLET;ORAL
01 10.0625MG
02 10.125MG
03 10.1875MG
04 10.25MG
05 10.375MG
06 10.5MG
07 2100MG
08 210MG
09 1150MG
10 1200MG
11 125MG
12 250MG
13 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
14 15MG
15 17.5MG
16 1EQ 0.1% BASE
17 2EQ 10MG BASE
18 1EQ 15MG BASE
19 1EQ 30MG BASE
01 5DISCN
02 18RX
RLD : Yes
TE Code : AB
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : UROXATRAL
Dosage Strength : 10MG
Approval Date : 2003-06-12
Application Number : 21287
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
Dosage Form : GEL; TOPICAL
Proprietary Name : PANRETIN
Dosage Strength : EQ 0.1% BASE
Approval Date : 1999-02-02
Application Number : 20886
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : LANOXIN
Dosage Strength : 0.0625MG
Approval Date : 1997-09-30
Application Number : 20405
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : LANOXIN
Dosage Strength : 0.125MG
Approval Date : 1997-09-30
Application Number : 20405
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : LANOXIN
Dosage Strength : 0.1875MG
Approval Date : 1997-09-30
Application Number : 20405
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : LANOXIN
Dosage Strength : 0.25MG
Approval Date : 1997-09-30
Application Number : 20405
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : LANOXIN
Dosage Strength : 0.375MG
Approval Date : 1997-09-30
Application Number : 20405
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : LANOXIN
Dosage Strength : 0.5MG
Approval Date : 1997-09-30
Application Number : 20405
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : PLAQUENIL
Dosage Strength : 200MG
Approval Date : 1982-01-01
Application Number : 9768
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : NILANDRON
Dosage Strength : 50MG
Approval Date : 1996-09-19
Application Number : 20169
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
