NDC 71335-1425 – Lansoprazole

Lansoprazole 30 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC71335-1425

Product details

Brand name
Lansoprazole
Generic name
Lansoprazole
Labeler
Bryant Ranch Prepack
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA205868
Marketed since
June 4, 2018
Listing expires
December 31, 2026
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Lansoprazole →

Package NDC codes (9)

Package NDCDescriptionSince
71335-1425-130 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1425-1)Dec 4, 2019
71335-1425-290 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1425-2)Nov 6, 2020
71335-1425-318 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1425-3)May 2, 2022
71335-1425-428 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1425-4)May 2, 2022
71335-1425-556 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1425-5)May 2, 2022
71335-1425-658 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1425-6)May 2, 2022
71335-1425-760 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1425-7)Sep 29, 2020
71335-1425-8180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1425-8)May 2, 2022
71335-1425-9120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1425-9)May 2, 2022

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