NDC 11673-915 – up and up omeprazole

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

Human Otc Drug

Product NDC11673-915

Product details

Brand name
up and up omeprazole
Generic name
Omeprazole
Labeler
Target Corporation
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
NDA · NDA022032
Marketed since
July 14, 2009
Listing expires
December 31, 2026
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for up and up omeprazole →

Package NDC codes (2)

Package NDCDescriptionSince
11673-915-011 BOTTLE in 1 CARTON (11673-915-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLEAug 13, 2013
11673-915-033 BOTTLE in 1 CARTON (11673-915-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLEAug 14, 2013

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