DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
GRANISETRON HYDROCHLORIDE
FDA Application No:
(ANDA) 078090
Active Ingredient(s):
GRANISETRON HYDROCHLORIDE
Company:
ABRAXIS PHARM
Label History
Labels are not available on this site for GRANISETRON HYDROCHLORIDE, (ANDA) 078090
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/3/2007
000
Tentative Approval
Therapeutic Equivalents
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