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: AB
Application Number: A209180
Product Number: 001
Approval Date: Jan 14, 2019
Applicant Holder Full Name: RISING PHARMA HOLDINGS INC
Marketing Status:
Prescription
Patent and Exclusivity Information