NDC 68788-8805 – Omeprazole

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

Human Prescription Drug

Product NDC68788-8805

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA078490
Marketed since
January 20, 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
68788-8805-1100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8805-1)Jan 20, 2025
68788-8805-220 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8805-2)Jan 20, 2025
68788-8805-330 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8805-3)Jan 20, 2025
68788-8805-414 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8805-4)Jan 20, 2025
68788-8805-660 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8805-6)Jan 20, 2025
68788-8805-7120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8805-7)Jan 20, 2025
68788-8805-990 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8805-9)Jan 20, 2025

Other Omeprazole products