01 1Shionogi
01 1POWDER;INTRAVENOUS
01 1RX
01 1FETROJA
01 1USA
Regulatory Info : RX
Registration Country : USA
Brand Name : FETROJA
Dosage Form : POWDER;INTRAVENOUS
Dosage Strength : EQ 1GM BASE/VIAL
Packaging :
Approval Date : 2019-11-14
Application Number : 209445
Regulatory Info : RX
Registration Country : USA
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