Naloxone Hydrochloride

Product NDC

52584-215

11-digit product format

525840215

Labeler code

52584

Product ID

52584-215_449ee750-6d89-4b31-b4aa-083b56f0dea5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Naloxone Hydrochloride

Dosage form

INJECTION, SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS

Labeler

General Injectables & Vaccines, Inc

Application

ANDA070256

Marketing category

ANDA

Marketing start

2010-08-01

Marketing end

0000-00-00

Substance

NALOXONE HYDROCHLORIDE

Active strength

0 mg/mL

Pharmacologic classes

Opioid Antagonist [EPC],Opioid Antagonists [MoA]

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record