NDC 68462-396 – Omeprazole

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

Human Prescription Drug

Product NDC68462-396

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
Glenmark Pharmaceuticals Inc., USA
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA091672
Marketed since
October 31, 2014
Listing expires
December 31, 2027
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Omeprazole →

Package NDC codes (4)

Package NDCDescriptionSince
68462-396-01100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68462-396-01)Oct 1, 2016
68462-396-101000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68462-396-10)Oct 1, 2016
68462-396-3030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68462-396-30)Oct 1, 2016
68462-396-9090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68462-396-90)Oct 1, 2016

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