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01 3FENOFIBRATE
02 4NEBIVOLOL HYDROCHLORIDE
03 3SERTRALINE HYDROCHLORIDE
04 3SILDENAFIL CITRATE
05 1TENOFOVIR DISOPROXIL FUMARATE
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01 3CAPSULE;ORAL
02 11TABLET;ORAL
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01 1134MG
02 1200MG
03 1300MG
04 167MG
05 2EQ 100MG BASE
06 1EQ 10MG BASE
07 1EQ 2.5MG BASE
08 1EQ 20MG BASE
09 2EQ 25MG BASE
10 2EQ 50MG BASE
11 1EQ 5MG BASE
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01 14RX
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RLD : No
TE Code : AB
Dosage Form : CAPSULE; ORAL
Proprietary Name : FENOFIBRATE (MICRONIZED)
Dosage Strength : 67MG
Approval Date : 2017-11-16
Application Number : 207805
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : CAPSULE; ORAL
Proprietary Name : FENOFIBRATE (MICRONIZED)
Dosage Strength : 134MG
Approval Date : 2017-11-16
Application Number : 207805
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : CAPSULE; ORAL
Proprietary Name : FENOFIBRATE (MICRONIZED)
Dosage Strength : 200MG
Approval Date : 2017-11-16
Application Number : 207805
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : NEBIVOLOL HYDROCHLORIDE
Dosage Strength : EQ 2.5MG BASE
Approval Date : 2021-12-17
Application Number : 212917
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : NEBIVOLOL HYDROCHLORIDE
Dosage Strength : EQ 5MG BASE
Approval Date : 2021-12-17
Application Number : 212917
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : NEBIVOLOL HYDROCHLORIDE
Dosage Strength : EQ 10MG BASE
Approval Date : 2021-12-17
Application Number : 212917
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : NEBIVOLOL HYDROCHLORIDE
Dosage Strength : EQ 20MG BASE
Approval Date : 2021-12-17
Application Number : 212917
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 25MG BASE
Approval Date : 2009-03-04
Application Number : 78677
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 : 2009-03-04
Application Number : 78677
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 : 2009-03-04
Application Number : 78677
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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