LANSOPRAZOLE

Product NDC

55700-393

11-digit product format

557000393

Labeler code

55700

Product ID

55700-393_ed81abd4-8868-4e7e-9636-5699dd46d885

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

LANSOPRAZOLE

Dosage form

CAPSULE, DELAYED RELEASE

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA201921

Marketing category

ANDA

Marketing start

2012-12-18

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