DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
STRIFON FORTE DSC
FDA Application No:
(ANDA) 081008
Active Ingredient(s):
CHLORZOXAZONE
Company:
FERNDALE LABS
Label History
Labels are not available on this site for STRIFON FORTE DSC, (ANDA) 081008
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/20/1991
003
Labeling
11/20/1991
002
Chemistry
11/20/1991
001
Chemistry
12/23/1988
000
Approval
Therapeutic Equivalents
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