Meclizine Hydrochloride

Product NDC

70518-0421

11-digit product format

705180421

Labeler code

70518

Product ID

70518-0421_84f738f1-0b46-45fd-e053-2991aa0aaad0

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

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