Meclizine Hydrochloride

Product NDC

0615-1554

11-digit product format

006151554

Labeler code

0615

Product ID

0615-1554_9ad2f9a6-2561-4c9a-b258-893596dfdfa8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

meclizine hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA087128

Marketing category

ANDA

Marketing start

1981-06-03

Marketing end

0000-00-00

Substance

MECLIZINE HYDROCHLORIDE

Active strength

25 mg/1

Pharmacologic classes

Antiemetic [EPC],Emesis Suppression [PE]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record