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) 077291
Active Ingredient(s):
CYCLOBENZAPRINE HYDROCHLORIDE
Company:
ACTAVIS TOTOWA
Label History
Labels are not available on this site for CYCLOBENZAPRINE HYDROCHLORIDE, (ANDA) 077291
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/4/2005
000
Tentative Approval
2/3/2006
000
Approval
Therapeutic Equivalents
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