NDC 31722-712 – Pantoprazole Sodium

Pantoprazole Sodium 20 mg/1 · Tablet, Delayed Release · Oral

Human Prescription Drug 2 recalls

Product NDC31722-712

Product details

Brand name
Pantoprazole Sodium
Generic name
Pantoprazole
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA202882
Marketed since
September 10, 2014
Listing expires
December 31, 2027
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
31722-712-3110 TABLET, DELAYED RELEASE in 1 BLISTER PACK (31722-712-31)Sep 10, 2014
31722-712-3210 TABLET, DELAYED RELEASE in 1 CARTON (31722-712-32)Sep 10, 2014
31722-712-9090 TABLET, DELAYED RELEASE in 1 BOTTLE (31722-712-90)Sep 10, 2014

Recalls mentioning this NDC

Other Pantoprazole Sodium products