Metoprolol Tartrate
METOPROLOL TARTRATE INJECTION, USP
Approved
Approval ID
b624095a-d1c1-1ce0-e053-2995a90a0698
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 4, 2023
Manufacturers
FDA
Medical Purchasing Solutions, LLC
DUNS: 601458529
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Metoprolol Tartrate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code71872-7225
Application NumberANDA077761
Product Classification
M
Marketing Category
C73584
G
Generic Name
Metoprolol Tartrate
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateMay 4, 2023
FDA Product Classification
INGREDIENTS (3)
SODIUM CHLORIDEInactive
Quantity: 45 mg in 5 mL
Code: 451W47IQ8X
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
METOPROLOL TARTRATEActive
Quantity: 5 mg in 5 mL
Code: W5S57Y3A5L
Classification: ACTIB