NDC 31722-571 – Lansoprazole

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

Human Prescription Drug

Product NDC31722-571

Product details

Brand name
Lansoprazole
Generic name
Lansoprazole
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA203083
Marketed since
May 18, 2020
Listing expires
December 31, 2026
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Lansoprazole →

Package NDC codes (5)

Package NDCDescriptionSince
31722-571-01100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-571-01)May 18, 2020
31722-571-05500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-571-05)May 18, 2020
31722-571-101000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-571-10)May 18, 2020
31722-571-3030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-571-30)May 18, 2020
31722-571-9090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-571-90)May 18, 2020

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