DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
NEO-MEDROL ACETATE
FDA Application No:
(ANDA) 060611
Active Ingredient(s):
METHYLPREDNISOLONE ACETATE; NEOMYCIN SULFATE
Company:
PHARMACIA AND UPJOHN
Label History
Labels are not available on this site for NEOMEDROL ACETATE, (ANDA) 060611
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/22/1993
005
Chemistry in Effect
9/13/1991
004
Chemistry
12/7/1964
000
Approval
There are no Therapeutic Equivalents
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