Meclizine Hydrochloride

Product NDC

68071-4352

11-digit product format

680714352

Labeler code

68071

Product ID

68071-4352_681b9198-b6e9-d17f-e053-2991aa0ac88c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Meclizine

Dosage form

TABLET

Route

ORAL

Labeler

NuCare Pharmaceuticals,Inc.

Application

ANDA201451

Marketing category

ANDA

Marketing start

2010-02-12

Marketing end

0000-00-00

Substance

MECLIZINE HYDROCHLORIDE

Active strength

13 mg/1

Pharmacologic classes

Antiemetic [EPC],Emesis Suppression [PE]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record