Meclizine Hydrochloride

Product NDC

51079-423

11-digit product format

510790423

Labeler code

51079

Product ID

51079-423_7cef7564-6c72-34a6-e053-2a91aa0ac2b0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Meclizine

Dosage form

TABLET

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA202640

Marketing category

ANDA

Marketing start

2014-10-13

Marketing end

2020-01-31

Substance

MECLIZINE HYDROCHLORIDE

Active strength

13 mg/1

Pharmacologic classes

Antiemetic [EPC],Emesis Suppression [PE]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record