NDC 68001-111 – Lansoprazole

Lansoprazole 15 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC68001-111

Product details

Brand name
Lansoprazole
Generic name
Lansoprazole
Labeler
BluePoint Laboratories
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA091269
Marketed since
December 1, 2013
Listing expires
December 31, 2026
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Lansoprazole →

Package NDC codes (2)

Package NDCDescriptionSince
68001-111-0430 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-111-04)Dec 1, 2013
68001-111-0590 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-111-05)Dec 1, 2013

Other Lansoprazole products