NDC 47335-615 – Norepinephrine Bitartrate

Norepinephrine Bitartrate 1 mg/mL · Injection, Solution, Concentrate · Intravenous

Human Prescription Drug 1 recall

Product NDC47335-615

Product details

Brand name
Norepinephrine Bitartrate
Generic name
Norepinephrine Bitartrate
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Injection, Solution, Concentrate
Route
Intravenous
Marketing category
ANDA · ANDA211980
Marketed since
July 1, 2021
Listing expires
December 31, 2026
Pharmacologic class
Catecholamine

Active ingredients

Uses, dosage, side effects and warnings for Norepinephrine Bitartrate →

Package NDC codes (1)

Package NDCDescriptionSince
47335-615-4410 VIAL, SINGLE-DOSE in 1 CARTON (47335-615-44) / 4 mL in 1 VIAL, SINGLE-DOSEJul 1, 2021

Recalls mentioning this NDC

Other Norepinephrine Bitartrate products