Active Ingredient: GRANISETRON HYDROCHLORIDE
Proprietary Name: GRANISOL
Dosage Form; Route of Administration: SOLUTION; ORAL
Strength: EQ 2MG BASE/10ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A078334
Product Number: 001
Approval Date: Feb 28, 2008
Applicant Holder Full Name: INTRA-SANA LABORATORIES LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information