RANITIDINE

Product NDC

61919-455

11-digit product format

619190455

Labeler code

61919

Product ID

61919-455_8ff018fe-3d15-55e5-e053-2995a90ab94d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

RANITIDINE

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Direct_Rx

Application

ANDA078542

Marketing category

ANDA

Marketing start

2019-08-12

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

2020-12-31

Current FDA listing

Historical FDA.report record