FDA Drug Approval, A087176, CHLORTHALIDONE

FDA Drug Approval, A087176, CHLORTHALIDONE

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ANDA: 087176
Company: IVAX PHARMS
Drug Name: CHLORTHALIDONE
Active Ingredients: CHLORTHALIDONE
Strength: 50MG
Dosage Form/Route: TABLET;ORAL
Action Date: 04/13/1981
Marketing Status: Discontinued
Submission Classification: ORIG-1 TE Code: None
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