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FDA Drug Approval, N020550, VALTREX
FDA Drug Approval, N020550, VALTREX
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NDA: 020550
Company: GLAXOSMITHKLINE
Drug Name: VALTREX
Active Ingredients: VALACYCLOVIR HYDROCHLORIDE
Strength: EQ 1GM BASE
Dosage Form/Route: TABLET; ORAL
Action Date: 12/15/1995
Marketing Status: Prescription
Submission Classification: Type 6 - New Indication (no longer used)
Company: GLAXOSMITHKLINE
Drug Name: VALTREX
Active Ingredients: VALACYCLOVIR HYDROCHLORIDE
Strength: EQ 1GM BASE
Dosage Form/Route: TABLET; ORAL
Action Date: 12/15/1995
Marketing Status: Prescription
Submission Classification: Type 6 - New Indication (no longer used)
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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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