DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
HYDROCHLOROTHIAZIDE
FDA Application No:
(ANDA) 085182
Active Ingredient(s):
HYDROCHLOROTHIAZIDE
Company:
HERITAGE PHARMS INC
Label History
Labels are not available on this site for HYDROCHLOROTHIAZIDE, (ANDA) 085182
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/17/1986
019
Chemistry
4/17/1986
018
Chemistry
11/29/1985
017
Chemistry
11/29/1985
016
Chemistry
11/29/1985
015
Chemistry
1/20/1978
000
Approval
Therapeutic Equivalents
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