Metoprolol Tartrate
These highlights do not include all the information needed to use METOPROLOL TARTRATE INJECTION safely and effectively. See full prescribing information for METOPROLOL TARTRATE INJECTION. METOPROLOL TARTRATE injection, for intravenous use Initial U.S. Approval: 1978
Approved
Approval ID
f0370951-ab26-d4d1-b857-57518f3c4175
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 27, 2023
Manufacturers
FDA
Almaject, Inc.
DUNS: 116626205
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 Code72611-740
Application NumberANDA204205
Product Classification
M
Marketing Category
C73584
G
Generic Name
metoprolol tartrate
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateOctober 15, 2020
FDA Product Classification
INGREDIENTS (3)
metoprolol tartrateActive
Quantity: 1 mg in 1 mL
Code: W5S57Y3A5L
Classification: ACTIB
sodium chlorideInactive
Quantity: 9 mg in 1 mL
Code: 451W47IQ8X
Classification: IACT
waterInactive
Code: 059QF0KO0R
Classification: IACT