DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
MANDOL
FDA Application No:
(ANDA) 062560
Active Ingredient(s):
CEFAMANDOLE NAFATE
Company:
LILLY
Label History
Labels are not available on this site for MANDOL, (ANDA) 062560
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/30/1992
005
Chemistry
11/23/1992
004
Chemistry
9/10/1985
000
Approval
Therapeutic Equivalents
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