NDC 62756-377 – Omeprazole

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

Human Otc Drug

Product NDC62756-377

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA207891
Marketed since
January 1, 2019
Listing expires
December 31, 2026
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Omeprazole →

Package NDC codes (6)

Package NDCDescriptionSince
62756-377-112 BOTTLE in 1 CARTON (62756-377-11) / 14 TABLET, DELAYED RELEASE in 1 BOTTLEJan 1, 2019
62756-377-123 BOTTLE in 1 CARTON (62756-377-12) / 14 TABLET, DELAYED RELEASE in 1 BOTTLEJan 1, 2019
62756-377-211 BOTTLE in 1 CARTON (62756-377-21) / 14 TABLET, DELAYED RELEASE in 1 BOTTLEJan 1, 2019
62756-377-701 BLISTER PACK in 1 CARTON (62756-377-70) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACKJan 1, 2019
62756-377-793 BLISTER PACK in 1 CARTON (62756-377-79) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACKJan 1, 2019
62756-377-962 BLISTER PACK in 1 CARTON (62756-377-96) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACKJan 1, 2019

Other Omeprazole products