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FDA Drug Approval, A208086, GLUCAGON
FDA Drug Approval, A208086, GLUCAGON
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ANDA: 208086
Company: AMPHASTAR PHARMS INC
Drug Name: GLUCAGON
Active Ingredients: GLUCAGON
Strength: 1MG/VIAL
Dosage Form/Route: INJECTABLE;INJECTION
Action Date: 12/28/2020
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: TBD
Company: AMPHASTAR PHARMS INC
Drug Name: GLUCAGON
Active Ingredients: GLUCAGON
Strength: 1MG/VIAL
Dosage Form/Route: INJECTABLE;INJECTION
Action Date: 12/28/2020
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: TBD
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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