Active Ingredient: FLURAZEPAM HYDROCHLORIDE
Proprietary Name: FLURAZEPAM HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 15MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A070454
Product Number: 001
Approval Date: Aug 4, 1986
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
