DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
GRANISETRON
FDA Application No:
(ANDA) 077186
Active Ingredient(s):
GRANISETRON HYDROCHLORIDE
Company:
BEDFORD LABS
Original Approval or Tentative Approval Date:
January 20, 2006
There are no Therapeutic Equivalents
Labels are not available
Approval History, Letters, Reviews and Related Documents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
GRANISETRON
GRANISETRON HYDROCHLORIDE
(1MG/ML) 4MG/4ML
INJECTABLE; INJECTION
Tentative Approval
No
None
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