NDC 68788-4141 – Lansoprazole

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

Human Prescription Drug

Product NDC68788-4141

Product details

Brand name
Lansoprazole
Generic name
Lansoprazole
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Capsule, Delayed Release Pellets
Route
Oral
Marketing category
ANDA · ANDA090763
Marketed since
August 12, 2026
Listing expires
December 31, 2027
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Lansoprazole →

Package NDC codes (3)

Package NDCDescriptionSince
68788-4141-330 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (68788-4141-3)Aug 12, 2026
68788-4141-660 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (68788-4141-6)Aug 12, 2026
68788-4141-990 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (68788-4141-9)Aug 12, 2026

Other Lansoprazole products