NDC 68071-2199 – Omeprazole

Omeprazole 40 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC68071-2199

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
NuCarePharmaceuticals, Inc.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA091672
Marketed since
October 31, 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
68071-2199-414 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-2199-4)Mar 29, 2017
68071-2199-660 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-2199-6)Mar 29, 2017
68071-2199-77 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-2199-7)Mar 29, 2017
68071-2199-990 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-2199-9)Mar 29, 2017

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