Famotidine

Product NDC

55154-7552

11-digit product format

551547552

Labeler code

55154

Product ID

55154-7552_10570b57-f003-402c-a95e-c4e7199fc8cf

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Famotidine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Cardinal Health

Application

ANDA075511

Marketing category

ANDA

Marketing start

2010-05-07

Marketing end

0000-00-00

Substance

FAMOTIDINE

Active strength

20 mg/1

Pharmacologic classes

Histamine H2 Re

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record