ZANTAC

Product NDC

0173-0393

11-digit product format

001730393

Labeler code

0173

Product ID

0173-0393_31834de5-78a9-449a-9c3a-ed2c6c69fb04

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ranitidine hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

GlaxoSmithKline LLC

Application

NDA018703

Marketing category

NDA

Marketing start

1989-10-01

Marketing end

2019-04-30

Substance

RANITIDINE HYDROCHLORIDE

Active strength

300 mg/1

Pharmacologic classes

Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record