FAMOTIDINE

Product NDC

63739-325

11-digit product format

637390325

Labeler code

63739

Product ID

63739-325_edaaaea9-819f-4f35-8a4c-9d45d5d82e6c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Famotidine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

McKesson Corporation

Application

ANDA075718

Marketing category

ANDA

Marketing start

2001-04-16

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

2019-12-31

Current FDA listing

Historical FDA.report record