Acid Reducer

Product NDC

51660-351

11-digit product format

516600351

Labeler code

51660

Product ID

51660-351_6fd5c3c1-2d0e-42d0-a6f6-5cf77823fa03

Type

HUMAN OTC DRUG

Nonproprietary name

Ranitidine

Dosage form

TABLET

Route

ORAL

Labeler

Ohm Laboratories Inc.

Application

ANDA200536

Marketing category

ANDA

Marketing start

2011-06-28

Marketing end

0000-00-00

Substance

RANITIDINE HYDROCHLORIDE

Active strength

150 mg/1

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record