NDC 57237-162 – Omeprazole

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

Human Prescription Drug

Product NDC57237-162

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
Rising Pharma Holdings, Inc.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA203270
Marketed since
August 19, 2015
Listing expires
December 31, 2026
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Omeprazole →

Package NDC codes (5)

Package NDCDescriptionSince
57237-162-01100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-162-01)Aug 19, 2015
57237-162-101000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-162-10)Aug 19, 2015
57237-162-3030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-162-30)Aug 19, 2015
57237-162-50500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-162-50)Aug 19, 2015
57237-162-9090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-162-90)Aug 19, 2015

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