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01 8SODIUM PHENYLBUTYRATE
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01 8FOR SUSPENSION;ORAL
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01 10.5GM/PACKET
02 11GM/PACKET
03 12GM/PACKET
04 13GM/PACKET
05 14GM/PACKET
06 15GM/PACKET
07 16.67GM/PACKET
08 16GM/PACKET
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01 8RX
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RLD : Yes
TE Code :
Dosage Form : FOR SUSPENSION; ORAL
Proprietary Name : OLPRUVA
Dosage Strength : 2GM/PACKET
Approval Date : 2022-12-22
Application Number : 214860
RX/OTC/DISCN : RX
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
Dosage Form : FOR SUSPENSION; ORAL
Proprietary Name : OLPRUVA
Dosage Strength : 3GM/PACKET
Approval Date : 2022-12-22
Application Number : 214860
RX/OTC/DISCN : RX
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
Dosage Form : FOR SUSPENSION; ORAL
Proprietary Name : OLPRUVA
Dosage Strength : 4GM/PACKET
Approval Date : 2022-12-22
Application Number : 214860
RX/OTC/DISCN : RX
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
Dosage Form : FOR SUSPENSION; ORAL
Proprietary Name : OLPRUVA
Dosage Strength : 5GM/PACKET
Approval Date : 2022-12-22
Application Number : 214860
RX/OTC/DISCN : RX
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
Dosage Form : FOR SUSPENSION; ORAL
Proprietary Name : OLPRUVA
Dosage Strength : 6GM/PACKET
Approval Date : 2022-12-22
Application Number : 214860
RX/OTC/DISCN : RX
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
Dosage Form : FOR SUSPENSION; ORAL
Proprietary Name : OLPRUVA
Dosage Strength : 6.67GM/PACKET
Approval Date : 2022-12-22
Application Number : 214860
RX/OTC/DISCN : RX
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
Dosage Form : FOR SUSPENSION; ORAL
Proprietary Name : OLPRUVA
Dosage Strength : 0.5GM/PACKET
Approval Date : 2025-10-10
Application Number : 214860
RX/OTC/DISCN : RX
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
Dosage Form : FOR SUSPENSION; ORAL
Proprietary Name : OLPRUVA
Dosage Strength : 1GM/PACKET
Approval Date : 2025-10-10
Application Number : 214860
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
