APPLICATION
ANDA070171
TYPE
ANDA
ORIGINAL APPROVAL
2004-07-29
LATEST ACTION
2004-07-29
ROUTE
INJECTION
DOSAGE FORM
INJECTABLE
MARKETING STATUS
Discontinued
Products
NALOXONE HYDROCHLORIDEDiscontinued
NALOXONE HYDROCHLORIDE 0.02MG/ML · INJECTABLE · INJECTION
Approval history
2004-07-29OriginalAP
2001-02-14Manufacturing (CMC) · Supplement 4AP
1995-12-22Manufacturing (CMC) · Supplement 3AP
1993-04-26Manufacturing (CMC) · Supplement 2AP
1992-11-19Labeling · Supplement 1AP
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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