Famotidine

Product NDC

68788-9549

11-digit product format

687889549

Labeler code

68788

Product ID

68788-9549_24a50c3e-62f9-4cc5-9875-99d50b7caa95

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Famotidine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA075786

Marketing category

ANDA

Marketing start

2013-12-30

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