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01 4FAMOTIDINE
02 2RANITIDINE HYDROCHLORIDE
03 2RANOLAZINE
04 3SUMATRIPTAN SUCCINATE
05 4TADALAFIL
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01 2TABLET, EXTENDED RELEASE;ORAL
02 13TABLET;ORAL
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01 210MG
02 11GM
03 12.5MG
04 320MG
05 140MG
06 1500MG
07 15MG
08 1EQ 100MG BASE
09 1EQ 150MG BASE
10 1EQ 25MG BASE
11 1EQ 300MG BASE
12 1EQ 50MG BASE
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01 2OTC
02 13RX
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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : FAMOTIDINE
Dosage Strength : 20MG
Approval Date : 2022-01-07
Application Number : 215630
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : FAMOTIDINE
Dosage Strength : 40MG
Approval Date : 2022-01-07
Application Number : 215630
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : FAMOTIDINE
Dosage Strength : 10MG
Approval Date : 2022-01-28
Application Number : 215822
RX/OTC/DISCN : OTC
RLD : No
TE Code :

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RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : FAMOTIDINE
Dosage Strength : 20MG
Approval Date : 2022-01-28
Application Number : 215822
RX/OTC/DISCN : OTC
RLD : No
TE Code :

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : RANITIDINE HYDROCHLORIDE
Dosage Strength : EQ 150MG BASE
Approval Date : 2019-01-31
Application Number : 211289
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : RANITIDINE HYDROCHLORIDE
Dosage Strength : EQ 300MG BASE
Approval Date : 2019-01-31
Application Number : 211289
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 : RANOLAZINE
Dosage Strength : 500MG
Approval Date : 2022-01-19
Application Number : 214035
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 : RANOLAZINE
Dosage Strength : 1GM
Approval Date : 2022-01-19
Application Number : 214035
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : SUMATRIPTAN SUCCINATE
Dosage Strength : EQ 25MG BASE
Approval Date : 2024-12-31
Application Number : 219036
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : SUMATRIPTAN SUCCINATE
Dosage Strength : EQ 50MG BASE
Approval Date : 2024-12-31
Application Number : 219036
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
