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01 4FENOFIBRATE
02 3METHOCARBAMOL
03 2SOLIFENACIN SUCCINATE
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01 9TABLET;ORAL
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01 110MG
02 1145MG
03 1160MG
04 11GM
05 148MG
06 1500MG
07 154MG
08 15MG
09 1750MG
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01 9RX
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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : FENOFIBRATE
Dosage Strength : 54MG
Approval Date : 2017-12-19
Application Number : 207803
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : FENOFIBRATE
Dosage Strength : 160MG
Approval Date : 2017-12-19
Application Number : 207803
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : FENOFIBRATE
Dosage Strength : 48MG
Approval Date : 2021-02-10
Application Number : 208476
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : FENOFIBRATE
Dosage Strength : 145MG
Approval Date : 2021-02-10
Application Number : 208476
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AA
Dosage Form : TABLET; ORAL
Proprietary Name : METHOCARBAMOL
Dosage Strength : 500MG
Approval Date : 2011-10-21
Application Number : 200958
RX/OTC/DISCN : RX
RLD : No
TE Code : AA

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RLD : No
TE Code : AA
Dosage Form : TABLET; ORAL
Proprietary Name : METHOCARBAMOL
Dosage Strength : 750MG
Approval Date : 2011-10-21
Application Number : 200958
RX/OTC/DISCN : RX
RLD : No
TE Code : AA

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : METHOCARBAMOL
Dosage Strength : 1GM
Approval Date : 2021-12-06
Application Number : 200958
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : SOLIFENACIN SUCCINATE
Dosage Strength : 5MG
Approval Date : 2019-05-20
Application Number : 210281
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : SOLIFENACIN SUCCINATE
Dosage Strength : 10MG
Approval Date : 2019-05-20
Application Number : 210281
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
