NDC 0781-2790 – Omeprazole

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

Human Prescription Drug

Product NDC0781-2790

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
Sandoz Inc
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA075757
Marketed since
January 28, 2003
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
0781-2790-01100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0781-2790-01)Jan 28, 2003
0781-2790-101000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0781-2790-10)Jan 28, 2003
0781-2790-3130 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0781-2790-31)Jan 28, 2003
0781-2790-9290 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0781-2790-92)Jan 28, 2003

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