DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
ZEFAZONE
FDA Application No:
(NDA) 050637
Active Ingredient(s):
CEFMETAZOLE SODIUM
Company:
PHARMACIA AND UPJOHN
Label History
Labels are not available on this site for ZEFAZONE, (NDA) 050637
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/30/1993
008
Labeling Revision
12/8/1993
005
Package Change
7/30/1993
004
Labeling Revision
9/29/1992
001
New or Modified Indication
12/11/1989
000
Approval
There are no Therapeutic Equivalents
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