Ranitidine

Product NDC

0904-6349

11-digit product format

009046349

Labeler code

0904

Product ID

0904-6349_4f0084e3-f200-41a4-838e-556e7017a38d

Type

HUMAN OTC DRUG

Nonproprietary name

Ranitidine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Major Pharmaceuticals

Application

ANDA201745

Marketing category

ANDA

Marketing start

2013-10-01

Marketing end

2019-11-30

Substance

RANITIDINE HYDROCHLORIDE

Active strength

75 mg/1

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record