01 1ALFUZOSIN HYDROCHLORIDE
02 1ALITRETINOIN
03 6DIGOXIN
04 3HYDROCHLOROTHIAZIDE; METOPROLOL SUCCINATE
05 1HYDROXYCHLOROQUINE SULFATE
06 2NILUTAMIDE
07 1PHENOXYBENZAMINE HYDROCHLORIDE
08 2PILOCARPINE HYDROCHLORIDE
09 1SODIUM POLYSTYRENE SULFONATE
10 1TRANYLCYPROMINE SULFATE
11 2TRIAMTERENE
12 3ZONISAMIDE
01 6CAPSULE;ORAL
02 1GEL;TOPICAL
03 1POWDER;ORAL, RECTAL
04 4TABLET, EXTENDED RELEASE;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
09 112.5MG;EQ 100MG TARTRATE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
10 112.5MG;EQ 25MG TARTRATE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
11 112.5MG;EQ 50MG TARTRATE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
12 1150MG
13 1200MG
14 125MG
15 1453.6GM/BOT **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
16 250MG
17 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
18 15MG
19 17.5MG
20 1EQ 0.1% BASE
21 1EQ 10MG BASE
01 9DISCN
02 15RX
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 :
HYDROCHLOROTHIAZIDE; METOPROLOL SUCCINATE
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : DUTOPROL
Dosage Strength : 12.5MG;EQ 25MG TARTRATE ...
Approval Date : 2006-08-28
Application Number : 21956
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
HYDROCHLOROTHIAZIDE; METOPROLOL SUCCINATE
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : DUTOPROL
Dosage Strength : 12.5MG;EQ 50MG TARTRATE ...
Approval Date : 2006-08-28
Application Number : 21956
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
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