lansoprazole

Product NDC

55700-616

11-digit product format

557000616

Labeler code

55700

Product ID

55700-616_26f46d57-c752-49c5-ac9a-a7f91142a183

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

lansoprazole

Dosage form

CAPSULE, DELAYED RELEASE PELLETS

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA202366

Marketing category

ANDA

Marketing start

2018-05-04

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

2020-12-31

Current FDA listing

Historical FDA.report record