Fexofenadine hydrochloride

Product NDC

62011-0314

11-digit product format

620110314

Labeler code

62011

Product ID

62011-0314_4ce4b7a8-c9e1-4587-8166-17e55bc4aeb4

Type

HUMAN OTC DRUG

Nonproprietary name

Fexofenadine hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Healthmart

Application

ANDA202039

Marketing category

ANDA

Marketing start

2016-10-14

Marketing end

0000-00-00

Substance

FEXOFENADINE HYDROCHLORIDE

Active strength

60 mg/1

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record