Allergy Relief

Product NDC

37205-745

11-digit product format

372050745

Labeler code

37205

Product ID

37205-745_7cafc926-850f-4d74-bd87-f5e45bc29600

Type

HUMAN OTC DRUG

Nonproprietary name

Loratadine

Dosage form

TABLET, ORALLY DISINTEGRATING

Route

ORAL

Labeler

Cardinal Health

Application

ANDA077153

Marketing category

ANDA

Marketing start

2007-08-31

Marketing end

0000-00-00

Substance

LORATADINE

Active strength

10 mg/1

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record