DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
CYCLOBENZAPRINE HYDROCHLORIDE
FDA Application No:
(ANDA) 073541
Active Ingredient(s):
CYCLOBENZAPRINE HYDROCHLORIDE
Company:
MUTUAL PHARM
Label History
Labels are not available on this site for CYCLOBENZAPRINE HYDROCHLORIDE, (ANDA) 073541
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/6/2006
007
Chemistry New Strength
4/6/2006
006
Chemistry New Strength
12/1/1998
001
Chemistry
5/23/1995
000
Approval
Therapeutic Equivalents
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