Fexofenadine Hydrochloride

Product NDC

0615-7636

11-digit product format

006157636

Labeler code

0615

Product ID

0615-7636_d2c9e88a-df18-4ba7-be45-13cf14b0d6c9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Fexofenadine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA076447

Marketing category

ANDA

Marketing start

2010-07-01

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

2017-12-31

Current FDA listing

Historical FDA.report record