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FDA Drug Approval, N006488, XYLOCAINE W/ EPINEPHRINE
FDA Drug Approval, N006488, XYLOCAINE W/ EPINEPHRINE
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NDA: 006488
Company: FRESENIUS KABI USA
Drug Name: XYLOCAINE W/ EPINEPHRINE
Active Ingredients: EPINEPHRINE; LIDOCAINE HYDROCHLORIDE
Strength: 0.005MG/ML;2%
Dosage Form/Route: INJECTABLE;INJECTION
Action Date: 11/19/1948
Marketing Status: Prescription
Submission Classification:
Company: FRESENIUS KABI USA
Drug Name: XYLOCAINE W/ EPINEPHRINE
Active Ingredients: EPINEPHRINE; LIDOCAINE HYDROCHLORIDE
Strength: 0.005MG/ML;2%
Dosage Form/Route: INJECTABLE;INJECTION
Action Date: 11/19/1948
Marketing Status: Prescription
Submission Classification:
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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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