Lansoprazole

Product NDC

50436-7350

11-digit product format

504367350

Labeler code

50436

Product ID

50436-7350_fdb5104b-cb42-452f-83a7-fd49c1363ae1

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Lansoprazole

Dosage form

CAPSULE, DELAYED RELEASE

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA077255

Marketing category

ANDA

Marketing start

2009-11-11

Marketing end

0000-00-00

Substance

LANSOPRAZOLE

Active strength

30 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record