acid reducer

Product NDC

41250-852

11-digit product format

412500852

Labeler code

41250

Product ID

41250-852_faa16f7c-5971-4294-b1f5-2eb1caa773ac

Type

HUMAN OTC DRUG

Nonproprietary name

Ranitidine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Meijer Distribution Inc

Application

ANDA091429

Marketing category

ANDA

Marketing start

2013-08-23

Marketing end

2021-01-31

Substance

RANITIDINE HYDROCHLORIDE

Active strength

150 mg/1

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record