NDC 70121-1719 – Magnesium Sulfate

Magnesium Sulfate Heptahydrate 40 mg/mL · Injection · Intravenous

Human Prescription Drug 1 recall

Product NDC70121-1719

Product details

Brand name
Magnesium Sulfate
Generic name
Magnesium Sulfate In Water For
Labeler
Amneal Pharmaceuticals LLC
Dosage form
Injection
Route
Intravenous
Marketing category
ANDA · ANDA216597
Marketed since
February 20, 2023
Listing expires
December 31, 2026
Pharmacologic class
Calculi Dissolution Agent; Osmotic Laxative

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
70121-1719-215 POUCH in 1 CARTON (70121-1719-2) / 1 BAG in 1 POUCH / 50 mL in 1 BAGJan 8, 2024
70121-1719-924 POUCH in 1 CARTON (70121-1719-9) / 1 BAG in 1 POUCH / 50 mL in 1 BAGFeb 20, 2023

Recalls mentioning this NDC

Other Magnesium Sulfate products