NDC 71205-907 – Omeprazole

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

Human Prescription Drug

Product NDC71205-907

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
Proficient Rx LP
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA212977
Marketed since
February 20, 2019
Listing expires
December 31, 2026
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Omeprazole →

Package NDC codes (6)

Package NDCDescriptionSince
71205-907-00100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-907-00)Jul 19, 2021
71205-907-111000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-907-11)Jul 19, 2021
71205-907-3030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-907-30)Jul 19, 2021
71205-907-55500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-907-55)Jul 19, 2021
71205-907-6060 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-907-60)Jul 19, 2021
71205-907-9090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-907-90)Jul 19, 2021

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