Ranitidine

Product NDC

42708-049

11-digit product format

427080049

Labeler code

42708

Product ID

42708-049_48a373a0-717f-41d9-a10a-da4691cd271a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ranitidine

Dosage form

TABLET

Route

ORAL

Labeler

QPharma Inc

Application

ANDA077824

Marketing category

ANDA

Marketing start

2009-12-16

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

2019-12-31

Current FDA listing

Historical FDA.report record