Active Ingredient: METOPROLOL TARTRATE
Proprietary Name: LOPRESSOR
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 1MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N018704
Product Number: 001
Approval Date: Mar 30, 1984
Applicant Holder Full Name: NOVARTIS PHARMACEUTICALS CORP
Marketing Status:
Discontinued
Patent and Exclusivity Information