Desloratadine

Product NDC

50268-218

11-digit product format

502680218

Labeler code

50268

Product ID

50268-218_652ee771-b54e-1a80-e053-2991aa0adb98

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Desloratadine

Dosage form

TABLET

Route

ORAL

Labeler

AvPAK

Application

ANDA078355

Marketing category

ANDA

Marketing start

2015-11-25

Marketing end

0000-00-00

Substance

DESLORATADINE

Active strength

5 mg/1

Pharmacologic classes

Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record