NDC 37808-915 – Omeprazole

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

Human Otc Drug

Product NDC37808-915

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
H E B
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
NDA · NDA022032
Marketed since
February 29, 2008
Listing expires
December 31, 2026
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Omeprazole →

Package NDC codes (3)

Package NDCDescriptionSince
37808-915-011 BOTTLE in 1 CARTON (37808-915-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLEFeb 4, 2011
37808-915-033 BOTTLE in 1 CARTON (37808-915-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLEApr 27, 2021
37808-915-302 CARTON in 1 CARTON (37808-915-30) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACKFeb 29, 2008

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