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01 2CLONIDINE
02 2FENOFIBRIC ACID
03 2METHOCARBAMOL
04 1RAMIPRIL
05 1TRAMADOL HYDROCHLORIDE
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01 2SOLUTION;ORAL
02 2SUSPENSION;ORAL
03 2TABLET, EXTENDED RELEASE;ORAL
04 2TABLET;ORAL
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01 1105MG
02 11MG/ML
03 135MG
04 15MG/ML
05 1750MG(5ML)
06 1750MG/5ML
07 1EQ 0.17MG BASE
08 1EQ 0.26MG BASE
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01 4DISCN
02 3RX
03 1Blank
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RLD : No
TE Code :
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : NEXICLON XR
Dosage Strength : EQ 0.17MG BASE
Approval Date : 2009-12-03
Application Number : 22500
RX/OTC/DISCN : RX
RLD : No
TE Code :

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RLD : No
TE Code :
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : NEXICLON XR
Dosage Strength : EQ 0.26MG BASE
Approval Date : 2009-12-03
Application Number : 22500
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

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RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : FIBRICOR
Dosage Strength : 35MG
Approval Date : 2009-08-14
Application Number : 22418
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : FIBRICOR
Dosage Strength : 105MG
Approval Date : 2009-08-14
Application Number : 22418
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
Dosage Form : SUSPENSION; ORAL
Proprietary Name : ATMEKSI
Dosage Strength : 750MG/5ML
Approval Date : 2025-07-30
Application Number : 219843
RX/OTC/DISCN : RX
RLD : Yes
TE Code :

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RLD :
TE Code :
Dosage Form : SUSPENSION; ORAL
Proprietary Name : ATMEKSI
Dosage Strength : 750MG(5ML)
Approval Date :
Application Number : 219843
RX/OTC/DISCN :
RLD :
TE Code :

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RLD : Yes
TE Code :
Dosage Form : SOLUTION; ORAL
Proprietary Name : VOSTALLY
Dosage Strength : 1MG/ML
Approval Date : 2025-07-23
Application Number : 219757
RX/OTC/DISCN : RX
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
Dosage Form : SOLUTION; ORAL
Proprietary Name : QDOLO
Dosage Strength : 5MG/ML
Approval Date : 2020-09-01
Application Number : 214044
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
