Naloxone Hydrochloride

Product NDC

55154-3954

11-digit product format

551543954

Labeler code

55154

Product ID

55154-3954_4575b897-3985-451e-b99b-2d36890dd4d4

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Naloxone Hydrochloride

Dosage form

INJECTION

Route

PARENTERAL

Labeler

Cardinal Health

Application

ANDA072076

Marketing category

ANDA

Marketing start

2001-06-01

Marketing end

2019-11-30

Substance

NALOXONE HYDROCHLORIDE

Active strength

1 mg/mL

Pharmacologic classes

Opioid Antagonist [EPC],Opioid Antagonists [MoA]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record