LANSOPRAZOLE

Product NDC

51991-771

11-digit product format

519910771

Labeler code

51991

Product ID

51991-771_a2884a15-5249-4f2e-ae9f-bbf2f942421e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

LANSOPRAZOLE

Dosage form

CAPSULE, DELAYED RELEASE

Route

ORAL

Labeler

Breckenridge Pharmaceutical, Inc.

Application

ANDA201921

Marketing category

ANDA

Marketing start

2012-12-18

Marketing end

2021-05-31

Substance

LANSOPRAZOLE

Active strength

15 mg/1

Pharmacologic classes

Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Inhibition Gastric Acid Secretion [PE]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record