NDC 51655-061 – Omeprazole

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

Human Prescription Drug

Product NDC51655-061

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
Northwind Health Company, LLC
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA075576
Marketed since
June 1, 2020
Listing expires
December 31, 2027
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Omeprazole →

Package NDC codes (3)

Package NDCDescriptionSince
51655-061-2560 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-061-25)Jun 1, 2020
51655-061-2690 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-061-26)Jan 25, 2024
51655-061-5230 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-061-52)Jun 1, 2020

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