Naloxone Hydrochloride

Product NDC

50090-3154

11-digit product format

500903154

Labeler code

50090

Product ID

50090-3154_d928dd37-eb87-4c38-af57-bb6d9d56cfbe

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Naloxone Hydrochloride

Dosage form

INJECTION

Route

PARENTERAL

Labeler

A-S Medication Solutions

Application

ANDA072076

Marketing category

ANDA

Marketing start

2001-06-01

Marketing end

0000-00-00

Substance

NALOXONE HYDROCHLORIDE

Active strength

1 mg/mL

Pharmacologic classes

Opioid Antagonist [EPC],Opioid Antagonists [MoA]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record