FDA Drug Approval, A087118, CHLORTHALIDONE
FDA Drug Approval, A087118, CHLORTHALIDONE
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ANDA: 087118
Company: SANDOZ
Drug Name: CHLORTHALIDONE
Active Ingredients: CHLORTHALIDONE
Strength: 50MG
Dosage Form/Route: TABLET;ORAL
Action Date: 09/16/1994
Marketing Status: Discontinued
Submission Classification: ORIG-1 TE Code: None
Company: SANDOZ
Drug Name: CHLORTHALIDONE
Active Ingredients: CHLORTHALIDONE
Strength: 50MG
Dosage Form/Route: TABLET;ORAL
Action Date: 09/16/1994
Marketing Status: Discontinued
Submission Classification: ORIG-1 TE Code: None