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FDA Drug Approval, N018930, METRONIDAZOLE
FDA Drug Approval, N018930, METRONIDAZOLE
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NDA: 018930
Company: CHARTWELL MOLECULES
Drug Name: METRONIDAZOLE
Active Ingredients: METRONIDAZOLE
Strength: 500MG
Dosage Form/Route: TABLET;ORAL
Action Date: 08/18/1983
Marketing Status: Discontinued
Submission Classification:
Company: CHARTWELL MOLECULES
Drug Name: METRONIDAZOLE
Active Ingredients: METRONIDAZOLE
Strength: 500MG
Dosage Form/Route: TABLET;ORAL
Action Date: 08/18/1983
Marketing Status: Discontinued
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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