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01 3AMLODIPINE BESYLATE
02 2CLOPIDOGREL BISULFATE
03 2DARIFENACIN HYDROBROMIDE
04 2MEMANTINE HYDROCHLORIDE
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01 2TABLET, EXTENDED RELEASE;ORAL
02 7TABLET;ORAL
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01 110MG
02 15MG
03 1EQ 10MG BASE
04 1EQ 15MG BASE
05 1EQ 2.5MG BASE
06 1EQ 300MG BASE
07 1EQ 5MG BASE
08 1EQ 7.5MG BASE
09 1EQ 75MG BASE
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01 9RX
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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : AMLODIPINE BESYLATE
Dosage Strength : EQ 2.5MG BASE
Approval Date : 2016-07-11
Application Number : 207821
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : AMLODIPINE BESYLATE
Dosage Strength : EQ 5MG BASE
Approval Date : 2016-07-11
Application Number : 207821
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : AMLODIPINE BESYLATE
Dosage Strength : EQ 10MG BASE
Approval Date : 2016-07-11
Application Number : 207821
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : CLOPIDOGREL BISULFATE
Dosage Strength : EQ 75MG BASE
Approval Date : 2020-07-17
Application Number : 213351
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : CLOPIDOGREL BISULFATE
Dosage Strength : EQ 300MG BASE
Approval Date : 2020-07-17
Application Number : 213351
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 : DARIFENACIN HYDROBROMIDE
Dosage Strength : EQ 7.5MG BASE
Approval Date : 2020-01-06
Application Number : 211045
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 : DARIFENACIN HYDROBROMIDE
Dosage Strength : EQ 15MG BASE
Approval Date : 2020-01-06
Application Number : 211045
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : MEMANTINE HYDROCHLORIDE
Dosage Strength : 5MG
Approval Date : 2020-12-11
Application Number : 210587
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : MEMANTINE HYDROCHLORIDE
Dosage Strength : 10MG
Approval Date : 2020-12-11
Application Number : 210587
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
