Famotidine

Product NDC

55154-5464

11-digit product format

551545464

Labeler code

55154

Product ID

55154-5464_d2a9b140-9433-44f8-a313-b94160415e85

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

famotidine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Cardinal Health

Application

ANDA075704

Marketing category

ANDA

Marketing start

2010-10-13

Marketing end

0000-00-00

Substance

FAMOTIDINE

Active strength

20 mg/1

Pharmacologic classes

Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record