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FDA Drug Approval, N016812, KETALAR
FDA Drug Approval, N016812, KETALAR
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NDA: 016812
Company: ENDO OPERATIONS
Drug Name: KETALAR
Active Ingredients: KETAMINE HYDROCHLORIDE
Strength: EQ 100MG BASE/ML
Dosage Form/Route: INJECTABLE;INJECTION
Action Date: 02/19/1970
Marketing Status: Prescription
Submission Classification: Type 1 - New Molecular Entity
Company: ENDO OPERATIONS
Drug Name: KETALAR
Active Ingredients: KETAMINE HYDROCHLORIDE
Strength: EQ 100MG BASE/ML
Dosage Form/Route: INJECTABLE;INJECTION
Action Date: 02/19/1970
Marketing Status: Prescription
Submission Classification: Type 1 - New Molecular Entity
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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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