MAXIMUM STRENGTH RANITIDINE

Product NDC

53943-018

11-digit product format

539430018

Labeler code

53943

Product ID

53943-018_525c9ed3-5af4-4405-8577-2b8ea3178c44

Type

HUMAN OTC DRUG

Nonproprietary name

Ranitidine

Dosage form

TABLET

Route

ORAL

Labeler

DISCOUNT DRUG MART

Application

ANDA207578

Marketing category

ANDA

Marketing start

2017-11-13

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