Fexofenadine Hydrochloride 180

Product NDC

0179-8325

11-digit product format

001798325

Labeler code

0179

Product ID

0179-8325_7b0985dd-c1a0-4829-e053-2991aa0a3e89

Type

HUMAN OTC DRUG

Nonproprietary name

Fexofenadine Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Kaiser Permanente

Application

ANDA076502

Marketing category

ANDA

Marketing start

2012-07-05

Marketing end

2020-02-29

Substance

FEXOFENADINE HYDROCHLORIDE

Active strength

180 mg/1

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record