Up and Up Ranitidine

Product NDC

11673-852

11-digit product format

116730852

Labeler code

11673

Product ID

11673-852_82c25793-1893-40b1-b24a-3dd2a5f3406c

Type

HUMAN OTC DRUG

Nonproprietary name

Ranitidine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Target Corporation

Application

ANDA091429

Marketing category

ANDA

Marketing start

2013-09-11

Marketing end

0000-00-00

Substance

RANITIDINE HYDROCHLORIDE

Active strength

150 mg/1

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record