NDC 0363-0915 – Omeprazole

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

Human Otc Drug

Product NDC0363-0915

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
Walgreen Company
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
NDA · NDA022032
Marketed since
February 27, 2008
Listing expires
December 31, 2026
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Omeprazole →

Package NDC codes (4)

Package NDCDescriptionSince
0363-0915-011 BOTTLE in 1 CARTON (0363-0915-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLEOct 6, 2010
0363-0915-033 BOTTLE in 1 CARTON (0363-0915-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLEMar 25, 2011
0363-0915-302 CARTON in 1 CARTON (0363-0915-30) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACKFeb 27, 2008
0363-0915-553 CARTON in 1 CARTON (0363-0915-55) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACKFeb 27, 2008

Other Omeprazole products