Active Ingredient: GRANISETRON HYDROCHLORIDE
Proprietary Name: GRANISETRON HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 1MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A078846
Product Number: 001
Approval Date: Feb 27, 2009
Applicant Holder Full Name: DR REDDYS LABORATORIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information