NDC 68788-6881 – Omeprazole

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

Human Prescription Drug

Product NDC68788-6881

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA091672
Marketed since
January 20, 2017
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
68788-6881-1100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-1)Jan 20, 2017
68788-6881-220 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-2)Jan 20, 2017
68788-6881-330 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-3)Jan 20, 2017
68788-6881-414 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-4)Jan 20, 2017
68788-6881-660 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-6)Jan 20, 2017
68788-6881-8120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-8)Jan 20, 2017
68788-6881-990 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-9)Jan 20, 2017

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