NDC 62175-114 – Omeprazole

Omeprazole 10 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug 1 recall

Product NDC62175-114

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
September 3, 2003
Listing expires
December 31, 2026
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Omeprazole →

Package NDC codes (4)

Package NDCDescriptionSince
62175-114-3230 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-114-32)Sep 3, 2003
62175-114-37100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-114-37)Sep 3, 2003
62175-114-4690 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-114-46)Sep 3, 2003
62175-114-4972000 CAPSULE, DELAYED RELEASE in 1 DRUM (62175-114-49)Sep 3, 2003

Recalls mentioning this NDC

Other Omeprazole products