Fexofenadine hydrochloride

Product NDC

70677-0007

11-digit product format

706770007

Labeler code

70677

Product ID

70677-0007_5e4eb9c5-018f-4121-99ce-9d44b86ee425

Type

HUMAN OTC DRUG

Nonproprietary name

Fexofenadine hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Sunmark

Application

ANDA202039

Marketing category

ANDA

Marketing start

2016-10-12

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