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FDA Drug Approval, N017681, HIPREX
FDA Drug Approval, N017681, HIPREX
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NDA: 017681
Company: SS PHARMA
Drug Name: HIPREX
Active Ingredients: METHENAMINE HIPPURATE
Strength: 1GM
Dosage Form/Route: TABLET;ORAL
Action Date: 09/09/1976
Marketing Status: Prescription
Submission Classification: Type 5 - New Formulation or New Manufacturer
Company: SS PHARMA
Drug Name: HIPREX
Active Ingredients: METHENAMINE HIPPURATE
Strength: 1GM
Dosage Form/Route: TABLET;ORAL
Action Date: 09/09/1976
Marketing Status: Prescription
Submission Classification: Type 5 - New Formulation or New Manufacturer
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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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