NDC 62175-136 – Omeprazole

Omeprazole 40 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug 1 recall

Product NDC62175-136

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
Lannett Company, Inc.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA075410
Marketed since
January 23, 2009
Listing expires
December 31, 2026
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Omeprazole →

Package NDC codes (5)

Package NDCDescriptionSince
62175-136-3230 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-136-32)Jan 23, 2009
62175-136-37100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-136-37)Jan 23, 2009
62175-136-431000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-136-43)Jan 23, 2009
62175-136-4690 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-136-46)Jan 23, 2009
62175-136-4936000 CAPSULE, DELAYED RELEASE in 1 DRUM (62175-136-49)Jan 23, 2009

Recalls mentioning this NDC

Other Omeprazole products