Meclizine Hydrochloride

Product NDC

70518-0422

11-digit product format

705180422

Labeler code

70518

Product ID

70518-0422_84fee638-38c8-152d-e053-2991aa0ad8cf

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Meclizine Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA200294

Marketing category

ANDA

Marketing start

2017-04-12

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