Famotidine

Product NDC

68645-141

11-digit product format

686450141

Labeler code

68645

Product ID

68645-141_78a293bc-11a7-4a4f-a2fa-254edd6e72a3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Famotidine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Legacy Pharmaceutical Packaging, LLC

Application

ANDA075511

Marketing category

ANDA

Marketing start

2009-10-26

Marketing end

2020-05-31

Substance

FAMOTIDINE

Active strength

40 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