NDC 68788-7742 – Lansoprazole

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

Human Prescription Drug

Product NDC68788-7742

Product details

Brand name
Lansoprazole
Generic name
Lansoprazole
Labeler
Preferred Pharmaceuticals, Inc.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA205868
Marketed since
July 1, 2020
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
68788-7742-114 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-1)Jul 1, 2020
68788-7742-330 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-3)Jul 1, 2020
68788-7742-660 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-6)Jul 1, 2020
68788-7742-8120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-8)Jul 1, 2020
68788-7742-990 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-9)Jul 1, 2020

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