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01 2MONTELUKAST SODIUM
02 3SERTRALINE HYDROCHLORIDE
03 4TOPIRAMATE
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01 2TABLET, CHEWABLE;ORAL
02 7TABLET;ORAL
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01 1100MG
02 1200MG
03 125MG
04 150MG
05 1EQ 100MG BASE
06 1EQ 25MG BASE
07 1EQ 4MG BASE
08 1EQ 50MG BASE
09 1EQ 5MG BASE
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01 2DISCN
02 7RX
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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 :

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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 :

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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

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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

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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

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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

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : TOPIRAMATE
Dosage Strength : 50MG
Approval Date : 2009-03-27
Application Number : 77733
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : TOPIRAMATE
Dosage Strength : 100MG
Approval Date : 2009-03-27
Application Number : 77733
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : TOPIRAMATE
Dosage Strength : 200MG
Approval Date : 2009-03-27
Application Number : 77733
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
