Leader Acid Control

Product NDC

49781-051

11-digit product format

497810051

Labeler code

49781

Product ID

49781-051_e8538b31-aa69-41d5-9cfd-05002e5bea7d

Type

HUMAN OTC DRUG

Nonproprietary name

Ranitidine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Cardinal Health

Application

ANDA091429

Marketing category

ANDA

Marketing start

2011-05-25

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