DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
ONDANSETRON HYDROCHLORIDE
FDA Application No:
(ANDA) 077112
Active Ingredient(s):
ONDANSETRON HYDROCHLORIDE
Company:
PLIVA HRVATSKA DOO
Label History
Labels are not available on this site for ONDANSETRON HYDROCHLORIDE, (ANDA) 077112
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/5/2006
000
Tentative Approval
1/10/2007
000
Tentative Approval
6/25/2007
000
Approval
Therapeutic Equivalents
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