Ranitidine

Product NDC

70518-0263

11-digit product format

705180263

Labeler code

70518

Product ID

70518-0263_9a7026fd-aa09-bb46-e053-2995a90a3c57

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ranitidine

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA077824

Marketing category

ANDA

Marketing start

2017-02-27

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