Active Ingredient: SODIUM NITROPRUSSIDE
Proprietary Name: NIPRIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 50MG/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N017546
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: HOFFMANN LA ROCHE INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
