NDC 50090-7472 – Omeprazole

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

Human Prescription Drug

Product NDC50090-7472

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
A-S Medication Solutions
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA078490
Marketed since
March 1, 2014
Listing expires
December 31, 2026
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Omeprazole →

Package NDC codes (8)

Package NDCDescriptionSince
50090-7472-030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-0)Dec 12, 2024
50090-7472-215 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-2)Dec 12, 2024
50090-7472-360 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-3)Dec 12, 2024
50090-7472-420 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-4)Dec 12, 2024
50090-7472-590 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-5)Dec 12, 2024
50090-7472-6200 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-6)Dec 12, 2024
50090-7472-7180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-7)Dec 12, 2024
50090-7472-87 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-8)Dec 12, 2024

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