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01 1BioLineRx
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01 1POWDER;SUBCUTANEOUS
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01 1RX
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01 1APHEXDA
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01 1USA
Regulatory Info : RX
Registration Country : USA
Brand Name : APHEXDA
Dosage Form : POWDER;SUBCUTANEOUS
Dosage Strength : EQ 62MG BASE/VIAL
Packaging :
Approval Date : 2023-09-08
Application Number : 217159
Regulatory Info : RX
Registration Country : USA