APPLICATION
ANDA074777
TYPE
ANDA
ORIGINAL APPROVAL
2005-03-02
LATEST ACTION
2010-01-28
ROUTE
INJECTION
DOSAGE FORM
INJECTABLE
MARKETING STATUS
Discontinued
Products
RANITIDINE HYDROCHLORIDEDiscontinued
RANITIDINE HYDROCHLORIDE EQ 25MG BASE/ML · INJECTABLE · INJECTION
Approval history
2010-01-28Labeling · Supplement 5AP
2009-06-18Labeling · Supplement 4AP
2006-02-15Labeling · Supplement 2AP
2005-03-02OriginalAP
Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.
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