NDC 0409-2168 – Magnesium Sulfate

Magnesium Sulfate Heptahydrate 500 mg/mL · Injection, Solution · Intramuscular, Intravenous

Human Prescription Drug 3 recalls

Product NDC0409-2168

Product details

Brand name
Magnesium Sulfate
Generic name
Magnesium Sulfate
Labeler
Hospira, Inc.
Dosage form
Injection, Solution
Route
Intramuscular, Intravenous
Marketing category
ANDA · ANDA202411
Marketed since
March 31, 2005
Listing expires
December 31, 2027
Pharmacologic class
Calculi Dissolution Agent; Osmotic Laxative

Active ingredients

Uses, dosage, side effects and warnings for Magnesium Sulfate →

Package NDC codes (1)

Package NDCDescriptionSince
0409-2168-7725 VIAL, PLASTIC in 1 TRAY (0409-2168-77) / 20 mL in 1 VIAL, PLASTIC (0409-2168-17)Mar 15, 2021

Recalls mentioning this NDC

Other Magnesium Sulfate products