NDC 68071-2734 – Lansoprazole

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

Human Prescription Drug

Product NDC68071-2734

Product details

Brand name
Lansoprazole
Generic name
Lansoprazole
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA203083
Marketed since
May 18, 2020
Listing expires
December 31, 2027
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Lansoprazole →

Package NDC codes (2)

Package NDCDescriptionSince
68071-2734-114 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-2734-1)Jul 1, 2026
68071-2734-660 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-2734-6)May 25, 2022

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