NDC 72559-014 – Omeprazole

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

Human Otc Drug

Product NDC72559-014

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
Little Pharma, Inc.
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA207891
Marketed since
July 15, 2020
Listing expires
December 31, 2027
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Omeprazole →

Package NDC codes (4)

Package NDCDescriptionSince
72559-014-063 BOTTLE in 1 CARTON (72559-014-06) / 14 TABLET, DELAYED RELEASE in 1 BOTTLEJul 15, 2020
72559-014-071 BOTTLE in 1 CARTON (72559-014-07) / 14 TABLET, DELAYED RELEASE in 1 BOTTLEJul 15, 2020
72559-014-093 CARTON in 1 PACKAGE, COMBINATION (72559-014-09) / 3 BOTTLE in 1 CARTON / 14 TABLET, DELAYED RELEASE in 1 BOTTLEMar 31, 2026
72559-014-364 CARTON in 1 PACKAGE, COMBINATION (72559-014-36) / 3 BOTTLE in 1 CARTON / 14 TABLET, DELAYED RELEASE in 1 BOTTLEJun 18, 2024

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