NDC 0008-0923 – Protonix I.V.

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

Human Prescription Drug 1 recall

Product NDC0008-0923

Product details

Brand name
Protonix I.V.
Generic name
Pantoprazole Sodium
Labeler
Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
Dosage form
Injection, Powder, For Solution
Route
Intravenous
Marketing category
NDA · NDA020988
Marketed since
May 1, 2001
Listing expires
December 31, 2026
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Protonix →

Package NDC codes (3)

Package NDCDescriptionSince
0008-0923-511 VIAL in 1 CARTON (0008-0923-51) / 10 mL in 1 VIALMay 1, 2001
0008-0923-5510 CARTON in 1 PACKAGE (0008-0923-55) / 1 VIAL in 1 CARTON / 10 mL in 1 VIALMay 1, 2001
0008-0923-6025 CARTON in 1 PACKAGE (0008-0923-60) / 1 VIAL in 1 CARTON / 10 mL in 1 VIALMay 1, 2001

Recalls mentioning this NDC

Other Protonix products