Lansoprazole

Product NDC

68016-132

11-digit product format

680160132

Labeler code

68016

Product ID

68016-132_2ebb0f82-143f-47f9-a2f2-4eac4adcc171

Type

HUMAN OTC DRUG

Nonproprietary name

Lansoprazole

Dosage form

CAPSULE, DELAYED RELEASE

Route

ORAL

Labeler

Chain Drug Consortium, LLC

Application

ANDA202727

Marketing category

ANDA

Marketing start

2012-07-06

Marketing end

0000-00-00

Substance

LANSOPRAZOLE

Active strength

15 mg/1

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record