Visitor Monitoring Drug History: HYDRODIURIL
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: HYDRODIURIL
FDA Application No: (NDA) 011835
Active Ingredient(s): HYDROCHLOROTHIAZIDE
Company: MERCK
 
Label History
 
Labels are not available on this site for HYDRODIURIL, (NDA) 011835
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
1/10/2002 064Manufacturing Change or Addition  
9/8/1997 062Manufacturing Change or Addition  
9/9/1997 061Control Supplement  
11/5/1998 060Labeling Revision  
2/8/1996 059Formulation Revision  
11/29/1995 058Manufacturing Change or Addition  
9/26/1994 057Manufacturing Change or Addition  
2/16/1994 056Labeling Revision  
6/29/1994 055Labeling Revision  
10/28/1992 053Labeling Revision  
10/28/1992 051Labeling Revision  
10/28/1992 044New Dosage Regimen  
2/24/1959 000Approval  
 
Therapeutic Equivalents
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