DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
AZULFIDINE
FDA Application No:
(ANDA) 086983
Active Ingredient(s):
SULFASALAZINE
Company:
PHARMACIA AND UPJOHN
Label History
Labels are not available on this site for AZULFIDINE, (ANDA) 086983
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/29/1980
000
Approval
Therapeutic Equivalents
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