NDC 55150-202 – Pantoprazole Sodium

Pantoprazole Sodium 40 mg/1 · Injection, Powder, For Solution · Intravenous

Human Prescription Drug 2 recalls

Product NDC55150-202

Product details

Brand name
Pantoprazole Sodium
Generic name
Pantoprazole Sodium
Labeler
Eugia US LLC
Dosage form
Injection, Powder, For Solution
Route
Intravenous
Marketing category
ANDA · ANDA205675
Marketed since
March 30, 2016
Listing expires
December 31, 2027
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Pantoprazole Sodium →

Package NDC codes (2)

Package NDCDescriptionSince
55150-202-1010 VIAL, SINGLE-DOSE in 1 CARTON (55150-202-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (55150-202-00)Mar 30, 2016
55150-202-2525 VIAL, SINGLE-DOSE in 1 CARTON (55150-202-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (55150-202-00)Mar 30, 2016

Recalls mentioning this NDC

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