NDC 0378-8030 – Lansoprazole

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

Human Prescription Drug 1 recall

Product NDC0378-8030

Product details

Brand name
Lansoprazole
Generic name
lansoprazole
Labeler
Mylan Pharmaceuticals Inc.
Dosage form
Capsule, Delayed Release Pellets
Route
Oral
Marketing category
ANDA · ANDA090763
Marketed since
November 10, 2009
Listing expires
December 31, 2026
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Lansoprazole →

Package NDC codes (3)

Package NDCDescriptionSince
0378-8030-05500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (0378-8030-05)Nov 10, 2009
0378-8030-7790 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (0378-8030-77)Nov 10, 2009
0378-8030-9330 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (0378-8030-93)Nov 10, 2009

Recalls mentioning this NDC

Other Lansoprazole products