NDC 82009-022 – Omeprazole

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

Human Prescription Drug 1 recall

Product NDC82009-022

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
Quallent Pharmaceuticals Health LLC
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA075576
Marketed since
November 15, 2022
Marketing end
August 30, 2028
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Omeprazole →

Package NDC codes (1)

Package NDCDescriptionSince
82009-022-101000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (82009-022-10)Nov 15, 2022

Recalls mentioning this NDC

Other Omeprazole products