NDC 63323-064 – Magnesium Sulfate

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

Human Prescription Drug 1 recall

Product NDC63323-064

Product details

Brand name
Magnesium Sulfate
Generic name
Magnesium Sulfate Heptahydrate
Labeler
Fresenius Kabi USA, LLC
Dosage form
Injection, Solution
Route
Intramuscular, Intravenous
Marketing category
NDA · NDA019316
Marketed since
August 8, 2000
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 (4)

Package NDCDescriptionSince
63323-064-0325 VIAL, SINGLE-DOSE in 1 CARTON (63323-064-03) / 2 mL in 1 VIAL, SINGLE-DOSE (63323-064-01)Aug 8, 2000
63323-064-1125 VIAL, SINGLE-DOSE in 1 TRAY (63323-064-11) / 10 mL in 1 VIAL, SINGLE-DOSE (63323-064-04)Aug 8, 2000
63323-064-2325 VIAL, GLASS in 1 TRAY (63323-064-23) / 2 mL in 1 VIAL, GLASS (63323-064-21)Aug 8, 2000
63323-064-4325 VIAL, GLASS in 1 TRAY (63323-064-43) / 2 mL in 1 VIAL, GLASS (63323-064-41)Aug 8, 2000

Recalls mentioning this NDC

Other Magnesium Sulfate products