NDC 0338-1719 – Magnesium Sulfate

Magnesium Sulfate Heptahydrate 4 g/50mL · Injection, Solution · Intravenous

Human Prescription Drug

Product NDC0338-1719

Product details

Brand name
Magnesium Sulfate
Generic name
Magnesium Sulfate Heptahydrate
Labeler
Baxter Healthcare Corporation
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
ANDA · ANDA211966
Marketed since
June 1, 2020
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
0338-1719-4040 BAG in 1 CARTON (0338-1719-40) / 50 mL in 1 BAGJun 1, 2020

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