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01 1PEGULICIANINE ACETATE
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01 1LUMICELL
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01 1POWDER;INTRAVENOUS
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01 1EQ 39MG BASE/VIAL
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01 1USA
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Regulatory Info : RX
Registration Country : USA
Dosage Form : POWDER;INTRAVENOUS
Brand Name : LUMISIGHT
Dosage Strength : EQ 39MG BASE/VIAL
Packaging :
Approval Date : 2024-04-17
Application Number : 214511
Regulatory Info : RX
Registration Country : USA
