Lansoprazole

Product NDC

63739-574

11-digit product format

637390574

Labeler code

63739

Product ID

63739-574_e62b20fc-af49-4cde-a44f-37e20e54616a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

lansoprazole

Dosage form

CAPSULE, DELAYED RELEASE

Route

ORAL

Labeler

McKesson Corporation dba SKY Packaging

Application

ANDA091269

Marketing category

ANDA

Marketing start

2012-09-21

Marketing end

0000-00-00

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

2020-12-31

Current FDA listing

Historical FDA.report record