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NALOXONE HYDROCHLORIDE

ANDA · Abbreviated New Drug Application (Generic) · Sponsor: MANKIND PHARMA · Approved 2024-02-29

Drug application

FDA Application #

ANDA218404

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

MANKIND PHARMA

Manufacturer

Lifestar Pharma LLC

First approval

2024-02-29

Source

Authoritative

Drugs@FDA application overview

Machine

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