NDC 68788-8621 – Lansoprazole

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

Human Prescription Drug

Product NDC68788-8621

Product details

Brand name
Lansoprazole
Generic name
Lansoprazole
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA203203
Marketed since
April 4, 2024
Listing expires
December 31, 2027
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Lansoprazole →

Package NDC codes (5)

Package NDCDescriptionSince
68788-8621-114 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8621-1)Apr 5, 2024
68788-8621-330 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8621-3)Apr 4, 2024
68788-8621-660 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8621-6)Apr 4, 2024
68788-8621-8120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8621-8)Apr 4, 2024
68788-8621-990 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8621-9)Apr 4, 2024

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