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01 2BUPROPION HYDROCHLORIDE
02 3CARBAMAZEPINE
03 3MONTELUKAST SODIUM
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01 2TABLET, CHEWABLE;ORAL
02 5TABLET, EXTENDED RELEASE;ORAL
03 1TABLET;ORAL
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01 1100MG
02 1150MG
03 1200MG
04 1300MG
05 1400MG
06 1EQ 10MG BASE
07 1EQ 4MG BASE
08 1EQ 5MG BASE
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01 8RX
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RLD : No
TE Code : AB3
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : BUPROPION HYDROCHLORIDE
Dosage Strength : 150MG
Approval Date : 2017-06-30
Application Number : 207224
RX/OTC/DISCN : RX
RLD : No
TE Code : AB3

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RLD : No
TE Code : AB3
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : BUPROPION HYDROCHLORIDE
Dosage Strength : 300MG
Approval Date : 2017-06-30
Application Number : 207224
RX/OTC/DISCN : RX
RLD : No
TE Code : AB3

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RLD : No
TE Code : AB
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : CARBAMAZEPINE
Dosage Strength : 100MG
Approval Date : 2021-09-30
Application Number : 212948
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : CARBAMAZEPINE
Dosage Strength : 200MG
Approval Date : 2021-09-30
Application Number : 212948
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : CARBAMAZEPINE
Dosage Strength : 400MG
Approval Date : 2021-09-30
Application Number : 212948
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : MONTELUKAST SODIUM
Dosage Strength : EQ 10MG BASE
Approval Date : 2016-01-12
Application Number : 205683
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET, CHEWABLE; ORAL
Proprietary Name : MONTELUKAST SODIUM
Dosage Strength : EQ 4MG BASE
Approval Date : 2015-11-05
Application Number : 205695
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET, CHEWABLE; ORAL
Proprietary Name : MONTELUKAST SODIUM
Dosage Strength : EQ 5MG BASE
Approval Date : 2015-11-05
Application Number : 205695
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
