NDC 62756-129 – Pantoprazole Sodium

Pantoprazole Sodium 40 mg/10mL · Injection, Powder, Lyophilized, For Solution · Intravenous

Human Prescription Drug 1 recall

Product NDC62756-129

Product details

Brand name
Pantoprazole Sodium
Generic name
Pantoprazole Sodium
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing category
ANDA · ANDA077674
Marketed since
September 1, 2019
Listing expires
December 31, 2026
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
62756-129-401 VIAL in 1 CARTON (62756-129-40) / 10 mL in 1 VIALSep 1, 2019
62756-129-4410 VIAL in 1 CARTON (62756-129-44) / 10 mL in 1 VIALSep 1, 2019
62756-129-4525 CARTON in 1 PACKAGE (62756-129-45) / 1 VIAL in 1 CARTON / 10 mL in 1 VIALSep 1, 2019

Recalls mentioning this NDC

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