NDC 68071-3007 – Omeprazole

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

Human Prescription Drug

Product NDC68071-3007

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
NuCare Pharmaceuticals,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 (6)

Package NDCDescriptionSince
68071-3007-228 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3007-2)Jun 27, 2018
68071-3007-330 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3007-3)Jun 27, 2018
68071-3007-414 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3007-4)Jun 27, 2018
68071-3007-660 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3007-6)Jun 27, 2018
68071-3007-8180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3007-8)Jun 27, 2018
68071-3007-990 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3007-9)Jun 27, 2018

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