Active Ingredient: ALOSETRON HYDROCHLORIDE
Proprietary Name: ALOSETRON HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 0.5MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A200652
Product Number: 001
Approval Date: May 4, 2015
Applicant Holder Full Name: HIKMA PHARMACEUTICALS USA INC
Marketing Status:
Discontinued
Patent and Exclusivity Information