Ranitidine

Product NDC

50090-0606

11-digit product format

500900606

Labeler code

50090

Product ID

50090-0606_56044c34-fb0e-43ea-a1be-918addd0fa4c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ranitidine

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

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

2019-12-31

Current FDA listing

Historical FDA.report record