NDC 68382-411 – Omeprazole

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

Human Prescription Drug

Product NDC68382-411

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
Zydus Pharmaceuticals USA Inc.
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
68382-411-01100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-411-01)Nov 23, 2012
68382-411-05500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-411-05)Nov 23, 2012
68382-411-0630 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-411-06)Nov 23, 2012
68382-411-101000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-411-10)Nov 23, 2012
68382-411-1690 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-411-16)Nov 23, 2012

Other Omeprazole products