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Naloxone Hydrochloride - 0409-1782-69 - (NALOXONE HYDROCHLORIDE)

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Drug Information of Naloxone Hydrochloride

Product NDC: 0409-1782
Proprietary Name: Naloxone Hydrochloride
Non Proprietary Name: NALOXONE HYDROCHLORIDE
Active Ingredient(s): .4    mg/mL & nbsp;   NALOXONE HYDROCHLORIDE
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Naloxone Hydrochloride

Product NDC: 0409-1782
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070172
Marketing Category: ANDA
Start Marketing Date: 20120306

Package Information of Naloxone Hydrochloride

Package NDC: 0409-1782-69
Package Description: 10 CARTRIDGE in 1 BOX (0409-1782-69) > 1 mL in 1 CARTRIDGE

NDC Information of Naloxone Hydrochloride

NDC Code 0409-1782-69
Proprietary Name Naloxone Hydrochloride
Package Description 10 CARTRIDGE in 1 BOX (0409-1782-69) > 1 mL in 1 CARTRIDGE
Product NDC 0409-1782
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name NALOXONE HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 20120306
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name NALOXONE HYDROCHLORIDE
Strength Number .4
Strength Unit mg/mL
Pharmaceutical Classes Opioid Antagonist [EPC],Opioid Antagonists [MoA]

Complete Information of Naloxone Hydrochloride


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