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FDA Drug Approval, A212424, PHYTONADIONE
FDA Drug Approval, A212424, PHYTONADIONE
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ANDA: 212424
Company: CIPLA
Drug Name: PHYTONADIONE
Active Ingredients: PHYTONADIONE
Strength: 10MG/ML
Dosage Form/Route: INJECTABLE;INJECTION
Action Date: 04/22/2022
Marketing Status: Discontinued
Submission Classification: ORIG-1 TE Code: None
Company: CIPLA
Drug Name: PHYTONADIONE
Active Ingredients: PHYTONADIONE
Strength: 10MG/ML
Dosage Form/Route: INJECTABLE;INJECTION
Action Date: 04/22/2022
Marketing Status: Discontinued
Submission Classification: ORIG-1 TE Code: None
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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