fexofenadine hydrochloride

Product NDC

35356-749

11-digit product format

353560749

Labeler code

35356

Product ID

35356-749_db967d98-be9f-4e8d-b5ab-438b1c002fa8

Type

HUMAN OTC DRUG

Nonproprietary name

fexofenadine hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC

Application

ANDA076447

Marketing category

ANDA

Marketing start

2011-04-14

Marketing end

0000-00-00

Substance

FEXOFENADINE HYDROCHLORIDE

Active strength

180 mg/1

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record