NDC 65841-759 – Omeprazole

Omeprazole 10 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC65841-759

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
Zydus Lifesciences Limited
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA091352
Marketed since
November 23, 2012
Listing expires
December 31, 2026
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Omeprazole →

Package NDC codes (5)

Package NDCDescriptionSince
65841-759-01100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-759-01)Nov 23, 2012
65841-759-05500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-759-05)Nov 23, 2012
65841-759-0630 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-759-06)Nov 23, 2012
65841-759-101000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-759-10)Nov 23, 2012
65841-759-1690 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-759-16)Nov 23, 2012

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