Active Ingredient: NESIRITIDE
Proprietary Name: NATRECOR
Dosage Form; Route of Administration: FOR SOLUTION; INTRAVENOUS
Strength: 1.5MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N020920
Product Number: 001
Approval Date: Aug 10, 2001
Applicant Holder Full Name: SCIOS LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
