Famotidine

Product NDC

51079-966

11-digit product format

510790966

Labeler code

51079

Product ID

51079-966_96261301-e7a2-3992-e053-2a95a90a1f54

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

famotidine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA075704

Marketing category

ANDA

Marketing start

2001-05-01

Marketing end

2020-02-29

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

0000-00-00

Current FDA listing

Historical FDA.report record