MECLIZINE HYDROCHLORIDE

Product NDC

70518-0447

11-digit product format

705180447

Labeler code

70518

Product ID

70518-0447_67ce9cd9-442f-e67e-e053-2a91aa0a5844

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Meclizine Hydrocloride

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA040659

Marketing category

ANDA

Marketing start

2017-04-20

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

2019-12-31

Current FDA listing

Historical FDA.report record