Ranitidine

Product NDC

66267-188

11-digit product format

662670188

Labeler code

66267

Product ID

66267-188_9cbdfc6e-5de4-f5fd-e053-2a95a90ad10b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ranitidine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA078542

Marketing category

ANDA

Marketing start

2008-11-19

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

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record