Ranitidine Hydrochloride

Product NDC

51079-879

11-digit product format

510790879

Labeler code

51079

Product ID

51079-879_09a6458e-e1e8-4640-9341-396676319125

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ranitidine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA074467

Marketing category

ANDA

Marketing start

1997-07-11

Marketing end

0000-00-00

Substance

RANITIDINE HYDROCHLORIDE

Active strength

150 mg/1

Pharmacologic classes

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

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record