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NALOXONE HYDROCHLORIDE

ANDA · Abbreviated New Drug Application (Generic) · Sponsor: STERINOVA INC · Approved 2026-08-18

Drug application

FDA Application #
ANDA219942
Application type
Abbreviated New Drug Application (Generic)
Brand name
NALOXONE HYDROCHLORIDE
Generic name
Naloxone Hydrochloride
Active ingredients
NALOXONE HYDROCHLORIDE
Dosage form
INJECTABLE
Route
INJECTION
Marketing status
Prescription
Sponsor
STERINOVA INC
First approval
2026-08-18

Source

Authoritative
Drugs@FDA application overview
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