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Naloxone Hydrochloride - 0548-1469-00 - (Naloxone Hydrochloride)

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Drug Information of Naloxone Hydrochloride

Product NDC: 0548-1469
Proprietary Name: Naloxone Hydrochloride
Non Proprietary Name: Naloxone Hydrochloride
Active Ingredient(s): 1    mg/mL & nbsp;   Naloxone Hydrochloride
Administration Route(s): PARENTERAL
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Naloxone Hydrochloride

Product NDC: 0548-1469
Labeler Name: Amphastar Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072076
Marketing Category: ANDA
Start Marketing Date: 19880401

Package Information of Naloxone Hydrochloride

Package NDC: 0548-1469-00
Package Description: 1 SYRINGE in 1 CARTON (0548-1469-00) > 2 mL in 1 SYRINGE

NDC Information of Naloxone Hydrochloride

NDC Code 0548-1469-00
Proprietary Name Naloxone Hydrochloride
Package Description 1 SYRINGE in 1 CARTON (0548-1469-00) > 2 mL in 1 SYRINGE
Product NDC 0548-1469
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naloxone Hydrochloride
Dosage Form Name INJECTION
Route Name PARENTERAL
Start Marketing Date 19880401
Marketing Category Name ANDA
Labeler Name Amphastar Pharmaceuticals, Inc.
Substance Name NALOXONE HYDROCHLORIDE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes Opioid Antagonist [EPC],Opioid Antagonists [MoA]

Complete Information of Naloxone Hydrochloride


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