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) 078392
Active Ingredient(s):
GRANISETRON HYDROCHLORIDE
Company:
TEVA PARENTERAL
Label History
Labels are not available on this site for GRANISETRON HYDROCHLORIDE, (ANDA) 078392
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/18/2007
000
Tentative Approval
There are no Therapeutic Equivalents
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