DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
TIZANIDINE HYDROCHLORIDE
FDA Application No:
(ANDA) 076281
Active Ingredient(s):
TIZANIDINE HYDROCHLORIDE
Company:
ACTAVIS TOTOWA
Label History
Labels are not available on this site for TIZANIDINE HYDROCHLORIDE, (ANDA) 076281
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/20/2003
000
Approval
Therapeutic Equivalents
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