Ranitidine

Product NDC

63187-686

11-digit product format

631870686

Labeler code

63187

Product ID

63187-686_78df6821-dd96-4014-81a7-bdcd55742826

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ranitidine

Dosage form

TABLET

Route

ORAL

Labeler

Proficient Rx LP

Application

ANDA077824

Marketing category

ANDA

Marketing start

2009-12-16

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