01 4FENOPROFEN CALCIUM
02 2MONTELUKAST SODIUM
03 3SERTRALINE HYDROCHLORIDE
04 4TOPIRAMATE
01 3CAPSULE;ORAL
02 2TABLET, CHEWABLE;ORAL
03 8TABLET;ORAL
01 1100MG
02 1200MG
03 125MG
04 150MG
05 1EQ 100MG BASE
06 1EQ 200MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
07 1EQ 25MG BASE
08 1EQ 300MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
09 1EQ 400MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
10 1EQ 4MG BASE
11 1EQ 50MG BASE
12 1EQ 5MG BASE
13 1EQ 600MG BASE
01 6DISCN
02 7RX
RLD : No
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : NALFON
Dosage Strength : EQ 300MG BASE **Federal ...
Approval Date : 1982-01-01
Application Number : 17604
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : NALFON
Dosage Strength : EQ 200MG BASE **Federal ...
Approval Date : 1982-01-01
Application Number : 17604
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : NALFON
Dosage Strength : EQ 400MG BASE **Federal ...
Approval Date : 2009-07-21
Application Number : 17604
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : FENOPROFEN CALCIUM
Dosage Strength : EQ 600MG BASE
Approval Date : 1988-08-17
Application Number : 72267
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET, CHEWABLE; ORAL
Proprietary Name : MONTELUKAST SODIUM
Dosage Strength : EQ 4MG BASE
Approval Date : 2012-08-03
Application Number : 91588
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET, CHEWABLE; ORAL
Proprietary Name : MONTELUKAST SODIUM
Dosage Strength : EQ 5MG BASE
Approval Date : 2012-08-03
Application Number : 91588
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : SERTRALINE HYDROCHLORIDE
Dosage Strength : EQ 25MG BASE
Approval Date : 2007-02-06
Application Number : 76882
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : SERTRALINE HYDROCHLORIDE
Dosage Strength : EQ 50MG BASE
Approval Date : 2007-02-06
Application Number : 76882
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : SERTRALINE HYDROCHLORIDE
Dosage Strength : EQ 100MG BASE
Approval Date : 2007-02-06
Application Number : 76882
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : TOPIRAMATE
Dosage Strength : 25MG
Approval Date : 2009-03-27
Application Number : 77733
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
