NDC 68788-8864 – Omeprazole

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

Human Prescription Drug

Product NDC68788-8864

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA075757
Marketed since
April 23, 2025
Listing expires
December 31, 2026
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Omeprazole →

Package NDC codes (7)

Package NDCDescriptionSince
68788-8864-1100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8864-1)Apr 23, 2025
68788-8864-220 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8864-2)Apr 23, 2025
68788-8864-330 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8864-3)Apr 23, 2025
68788-8864-414 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8864-4)Apr 23, 2025
68788-8864-660 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8864-6)Apr 23, 2025
68788-8864-8120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8864-8)Apr 23, 2025
68788-8864-990 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8864-9)Apr 23, 2025

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