NDC 85509-1644 – Omeprazole

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

Human Prescription Drug

Product NDC85509-1644

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
PHOENIX RX LLC
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA078490
Marketed since
March 6, 2025
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
85509-1644-1120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (85509-1644-1)Jul 29, 2025
85509-1644-330 CAPSULE, DELAYED RELEASE in 1 BOTTLE (85509-1644-3)Jul 29, 2025
85509-1644-660 CAPSULE, DELAYED RELEASE in 1 BOTTLE (85509-1644-6)Jul 29, 2025
85509-1644-990 CAPSULE, DELAYED RELEASE in 1 BOTTLE (85509-1644-9)Jul 29, 2025

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