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NALOXONE

ANDA · Abbreviated New Drug Application (Generic) · Sponsor: HIKMA · Approved 1985-10-22

Drug application

FDA Application #

ANDA070298

Application type

Abbreviated New Drug Application (Generic)

Brand name

NALOXONE

Generic name

Naloxone Hydrochloride

Active ingredients

NALOXONE HYDROCHLORIDE

Dosage form

INJECTABLE

Route

INJECTION

Marketing status

Discontinued

Sponsor

HIKMA

First approval

1985-10-22

Source

Authoritative

Drugs@FDA application overview

Machine

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