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NALOXONE

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

Drug application

FDA Application #

ANDA070299

Application type

Abbreviated New Drug Application (Generic)

Brand name

NALOXONE

Generic name

NALXONE HYDROCHLORIDE

Active ingredients

NALOXONE HYDROCHLORIDE

Dosage form

INJECTABLE

Route

INJECTION

Marketing status

Prescription

Sponsor

HIKMA

Manufacturer

Hikma Pharmaceuticals USA Inc.

First approval

1985-10-22

Source

Authoritative

Drugs@FDA application overview

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