Naloxone Hydrochloride

Product NDC

55154-6980

11-digit product format

551546980

Labeler code

55154

Product ID

55154-6980_09bdd6dd-5680-414f-9232-b4120fae39a6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

NALOXONE HYDROCHLORIDE

Dosage form

INJECTION, SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS

Labeler

Cardinal Health

Application

ANDA070256

Marketing category

ANDA

Marketing start

2011-07-08

Marketing end

0000-00-00

Substance

NALOXONE HYDROCHLORIDE

Active strength

0 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