Meclizine Hydrochloride

Product NDC

71335-0189

11-digit product format

713350189

Labeler code

71335

Product ID

71335-0189_d31b133c-f2f5-4954-a722-dca52d46f58d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Meclizine Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA200294

Marketing category

ANDA

Marketing start

2012-04-30

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

2019-12-31

Current FDA listing

Historical FDA.report record