NDC 57237-161 – Omeprazole

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

Human Prescription Drug

Product NDC57237-161

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
57237-161-01100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-161-01)Aug 19, 2015
57237-161-3030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-161-30)Aug 19, 2015
57237-161-50500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-161-50)Aug 19, 2015
57237-161-9090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-161-90)Aug 19, 2015
57237-161-991000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-161-99)Aug 19, 2015

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