RANITIDINE HYDROCHLORIDE

Product NDC

61919-199

11-digit product format

619190199

Labeler code

61919

Product ID

61919-199_9cad1a67-25d3-4da8-e053-2a95a90a6abd

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

RANITIDINE HYDROCHLORIDE

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Direct Rx

Application

ANDA077824

Marketing category

ANDA

Marketing start

2017-11-06

Marketing end

0000-00-00

Substance

RANITIDINE HYDROCHLORIDE

Active strength

300 mg/1

Pharmacologic classes

Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record