Active Ingredient: RIMANTADINE HYDROCHLORIDE
Proprietary Name: FLUMADINE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 100MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019649
Product Number: 001
Approval Date: Sep 17, 1993
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information