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FDA Drug Approval, A087029, CHLORTHALIDONE
FDA Drug Approval, A087029, CHLORTHALIDONE
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ANDA: 087029
Company: WATSON LABS
Drug Name: CHLORTHALIDONE
Active Ingredients: CHLORTHALIDONE
Strength: 50MG
Dosage Form/Route: TABLET;ORAL
Action Date: 01/00/1900
Marketing Status: Discontinued
Submission Classification: TE Code: None
Company: WATSON LABS
Drug Name: CHLORTHALIDONE
Active Ingredients: CHLORTHALIDONE
Strength: 50MG
Dosage Form/Route: TABLET;ORAL
Action Date: 01/00/1900
Marketing Status: Discontinued
Submission Classification: TE Code: None
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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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