DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
ISONIAZID
FDA Application No:
(ANDA) 080132
Active Ingredient(s):
ISONIAZID
Company:
PUREPAC PHARM
Label History
Labels are not available on this site for ISONIAZID, (ANDA) 080132
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/9/1985
018
Chemistry
7/14/1982
015
Chemistry
3/4/1982
013
Chemistry
Therapeutic Equivalents
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