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) 076559
Active Ingredient(s):
ONDANSETRON HYDROCHLORIDE
Company:
DR REDDYS LABS LTD
Label History
Labels are not available on this site for ONDANSETRON HYDROCHLORIDE, (ANDA) 076559
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/26/2006
000
Approval
Letter
There are no Therapeutic Equivalents
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