Naloxone Hydrochloride

Product NDC

52584-469

11-digit product format

525840469

Labeler code

52584

Product ID

52584-469_b0cd3762-ad86-42ce-8995-4ec68f3a09a6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Naloxone Hydrochloride

Dosage form

INJECTION

Route

PARENTERAL

Labeler

General Injectables & Vaccines, Inc.

Application

ANDA072076

Marketing category

ANDA

Marketing start

2010-12-27

Marketing end

0000-00-00

Substance

NALOXONE HYDROCHLORIDE

Active strength

1 mg/mL

Pharmacologic classes

Opioid Antagonist [EPC],Opioid Antagonists [MoA]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record