NDC 49999-265 – Omeprazole

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

Human Prescription Drug

Product NDC49999-265

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
Quality Care Products, LLC
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA075576
Marketed since
October 13, 2010
Marketing end
January 31, 2027
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Omeprazole →

Package NDC codes (3)

Package NDCDescriptionSince
49999-265-3030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49999-265-30)Nov 1, 2013
49999-265-6060 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49999-265-60)Nov 1, 2013
49999-265-9090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49999-265-90)Nov 1, 2013

Other Omeprazole products