Leader Acid Control

Product NDC

49781-079

11-digit product format

497810079

Labeler code

49781

Product ID

49781-079_3cdb4406-8a0b-4783-aab1-848b73f7629d

Type

HUMAN OTC DRUG

Nonproprietary name

Ranitidine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Cardinal Health

Application

ANDA091429

Marketing category

ANDA

Marketing start

2014-03-11

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