Childrens Allergy

Product NDC

63868-096

11-digit product format

638680096

Labeler code

63868

Product ID

63868-096_80415a08-ac92-4b50-8c49-33a0a631a937

Type

HUMAN OTC DRUG

Nonproprietary name

Loratadine

Dosage form

LIQUID

Route

ORAL

Labeler

QUALITY CHOICE (Chain Drug Marketing Association)

Application

ANDA077421

Marketing category

ANDA

Marketing start

2015-01-31

Marketing end

2020-12-31

Substance

LORATADINE

Active strength

5 mg/5mL

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record