NDC 55111-399 – Lansoprazole

Lansoprazole 30 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug 2 recalls

Product NDC55111-399

Product details

Brand name
Lansoprazole
Generic name
Lansoprazole
Labeler
Dr.Reddy's Laboratories Ltd.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA091269
Marketed since
October 15, 2010
Listing expires
December 31, 2026
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Lansoprazole →

Package NDC codes (6)

Package NDCDescriptionSince
55111-399-01100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-399-01)Oct 15, 2010
55111-399-05500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-399-05)Oct 15, 2010
55111-399-3030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-399-30)Oct 15, 2010
55111-399-6060 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-399-60)Oct 15, 2010
55111-399-791 BLISTER PACK in 1 CARTON (55111-399-79) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACKOct 15, 2010
55111-399-9090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-399-90)Oct 15, 2010

Recalls mentioning this NDC

Other Lansoprazole products