lansoprazole

Product NDC

50268-466

11-digit product format

502680466

Labeler code

50268

Product ID

50268-466_9ba9c54c-9481-1b92-e053-2995a90a151d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

lansoprazole

Dosage form

CAPSULE, DELAYED RELEASE PELLETS

Route

ORAL

Labeler

AvPAK

Application

ANDA202366

Marketing category

ANDA

Marketing start

2016-07-14

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

2021-12-31

Current FDA listing

Historical FDA.report record