MECLIZINE HYDROCHLORIDE

Product NDC

50436-3986

11-digit product format

504363986

Labeler code

50436

Product ID

50436-3986_47f33965-7ea2-4bd1-9b4b-72a6653a7bcd

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Meclizine Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA040659

Marketing category

ANDA

Marketing start

2010-06-04

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