NDC 82009-183 – Omeprazole

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

Human Prescription Drug

Product NDC82009-183

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
Quallent Pharmaceuticals Health LLC
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA078490
Marketed since
November 15, 2025
Listing expires
December 31, 2026
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Omeprazole →

Package NDC codes (1)

Package NDCDescriptionSince
82009-183-101000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (82009-183-10)Nov 15, 2025

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