NDC 68071-3572 – Lansoprazole

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

Human Prescription Drug

Product NDC68071-3572

Product details

Brand name
Lansoprazole
Generic name
Lansoprazole
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA203203
Marketed since
August 24, 2018
Listing expires
December 31, 2026
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Lansoprazole →

Package NDC codes (1)

Package NDCDescriptionSince
68071-3572-414 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3572-4)Feb 12, 2024

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