Meclizine Hydrochloride

Product NDC

50090-2048

11-digit product format

500902048

Labeler code

50090

Product ID

50090-2048_c032f1db-847f-44cf-9d93-6453d41b99f1

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Meclizine

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA202640

Marketing category

ANDA

Marketing start

2012-09-19

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