NDC 0781-2859 – Omeprazole

Omeprazole 10 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC0781-2859

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
Sandoz Inc
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA075757
Marketed since
July 1, 2019
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
0781-2859-01100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0781-2859-01)Aug 1, 2019
0781-2859-101000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0781-2859-10)Aug 1, 2019
0781-2859-3130 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0781-2859-31)Aug 1, 2019
0781-2859-9290 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0781-2859-92)Jul 1, 2019

Other Omeprazole products