7 Select Acid Reducer

Product NDC

10202-852

11-digit product format

102020852

Labeler code

10202

Product ID

10202-852_340dc7ea-4120-404e-bf97-9b56f71505f7

Type

HUMAN OTC DRUG

Nonproprietary name

Ranitidine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

7-Eleven

Application

ANDA091429

Marketing category

ANDA

Marketing start

2014-04-22

Marketing end

2020-11-30

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