Fexofenadine Hydrochloride

Product NDC

0904-5962

11-digit product format

009045962

Labeler code

0904

Product ID

0904-5962_42579609-eccc-473c-8dd9-a94b94a74832

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Fexofenadine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Major Pharmaceuticals

Application

ANDA076502

Marketing category

ANDA

Marketing start

2009-06-10

Marketing end

0000-00-00

Substance

FEXOFENADINE HYDROCHLORIDE

Active strength

60 mg/1

Pharmacologic classes

Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record