Fexofenadine hydrochloride

Product NDC

42291-296

11-digit product format

422910296

Labeler code

42291

Product ID

42291-296_636342f3-9a9f-ba62-e053-2a91aa0ace17

Type

HUMAN OTC DRUG

Nonproprietary name

Fexofenadine hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

AvKARE, Inc.

Application

ANDA202039

Marketing category

ANDA

Marketing start

2015-10-16

Marketing end

0000-00-00

Substance

FEXOFENADINE HYDROCHLORIDE

Active strength

60 mg/1

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record