NDC 0093-7351 – Lansoprazole

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

Human Prescription Drug

Product NDC0093-7351

Product details

Brand name
Lansoprazole
Generic name
Lansoprazole
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA077255
Marketed since
November 11, 2009
Marketing end
June 30, 2027
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Lansoprazole →

Package NDC codes (1)

Package NDCDescriptionSince
0093-7351-5630 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0093-7351-56)Nov 11, 2009

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