NDC 68071-3733 – Omeprazole

Omeprazole 20 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC68071-3733

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA078490
Marketed since
March 1, 2014
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
68071-3733-220 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3733-2)Sep 29, 2025
68071-3733-330 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3733-3)Jan 14, 2025
68071-3733-660 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3733-6)Mar 3, 2025
68071-3733-990 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3733-9)Dec 2, 2024

Other Omeprazole products