Acid Reducer

Product NDC

51660-352

11-digit product format

516600352

Labeler code

51660

Product ID

51660-352_1a199803-a059-40ce-8a16-f43cca12e38f

Type

HUMAN OTC DRUG

Nonproprietary name

Ranitidine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Ohm Laboratories Inc.

Application

ANDA201745

Marketing category

ANDA

Marketing start

2012-07-10

Marketing end

0000-00-00

Substance

RANITIDINE HYDROCHLORIDE

Active strength

75 mg/1

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record