Visitor Monitoring Drug History: ORETIC
 
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: ORETIC
FDA Application No: (NDA) 011971
Active Ingredient(s): HYDROCHLOROTHIAZIDE
Company: ABBOTT
 
Label History
 
Labels are not available on this site for ORETIC, (NDA) 011971
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/16/1998 027Package Change  
10/23/1986 026Manufacturing Change or Addition  
10/22/1986 026Control Supplement  
7/15/1985 025Control Supplement  
12/15/1983 024Manufacturing Change or Addition  
5/14/1982 023Manufacturing Change or Addition  
6/11/1982 022Control Supplement  
9/13/1991 021Practioner Draft Labeling  
6/29/1976 016Control Supplement  
2/3/1976 015Labeling Revision  
3/3/1975 012Labeling Revision  
7/6/1959 000Approval  
 
Therapeutic Equivalents
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