Meclizine Hydrochloride

Product NDC

66267-139

11-digit product format

662670139

Labeler code

66267

Product ID

66267-139_9cadc5c4-8785-3aee-e053-2995a90a8040

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Meclizine Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA200294

Marketing category

ANDA

Marketing start

2012-04-30

Marketing end

0000-00-00

Substance

MECLIZINE HYDROCHLORIDE

Active strength

25 mg/1

Pharmacologic classes

Antiemetic [EPC],Emesis Suppression [PE]

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record