APPLICATION
ANDA071811
TYPE
ANDA
ORIGINAL APPROVAL
1988-07-19
LATEST ACTION
1994-04-08
ROUTE
INJECTION
DOSAGE FORM
INJECTABLE
MARKETING STATUS
Discontinued
Products
NALOXONE HYDROCHLORIDEDiscontinued
NALOXONE HYDROCHLORIDE 0.4MG/ML · INJECTABLE · INJECTION
Approval history
1994-04-08Labeling · Supplement 4AP
1988-07-19OriginalAP
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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