APPLICATION
ANDA070189
TYPE
ANDA
ORIGINAL APPROVAL
1985-10-02
LATEST ACTION
1988-01-22
ROUTE
INJECTION
DOSAGE FORM
INJECTABLE
MARKETING STATUS
Discontinued
Products
NALOXONEDiscontinued
NALOXONE HYDROCHLORIDE 0.02MG/ML · INJECTABLE · INJECTION
Approval history
1988-01-22Manufacturing (CMC) · Supplement 2AP
1987-06-05Manufacturing (CMC) · Supplement 4AP
1987-02-20Manufacturing (CMC) · Supplement 3AP
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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