Meclizine Hydrochloride

Product NDC

60429-205

11-digit product format

604290205

Labeler code

60429

Product ID

60429-205_79f3f684-da4e-a36e-e053-2991aa0a0408

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

meclizine hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Golden State Medical Supply, Inc.

Application

ANDA087128

Marketing category

ANDA

Marketing start

2012-04-02

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

2020-12-31

Current FDA listing

Historical FDA.report record