NDC Code(s) : 72611-740-01, 72611-740-10
Packager : Almaject, Inc.

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Metoprolol Tartratemetoprolol tartrate INJECTION, SOLUTION
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72611-740
Route of Administration INTRAVENOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
metoprolol tartrate(UNII: W5S57Y3A5L)
(metoprolol - UNII:GEB06NHM23) 		metoprolol tartrate1 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
sodium chloride(UNII: 451W47IQ8X)9 mg in 1 mL
water(UNII: 059QF0KO0R)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:72611-740-1010 in 1 CARTON 31/03/2020
1NDC:72611-740-015 mL in 1 VIAL, SINGLE-DOSE Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA204205 03/31/2020

LABELER - Almaject, Inc.(116626205)

PRINCIPAL DISPLAY PANEL


NDC 68083-131-01        Rx only
Metoprolol Tartrate Injection, USP
5 mg per 5 mL (1 mg/mL)
FOR INTRAVENOUS USE
Vial Label

metoprolol-label


PRINCIPAL DISPLAY PANEL

NDC 72611-740-10

Metoprolol Tartrate Injection, USP

5 mg/5 mL

(1 mg/mL)

For Intravenous Use

Sterile