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Naloxone Hydrochloride - 52584-215-01 - (Naloxone Hydrochloride)

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Drug Information of Naloxone Hydrochloride

Product NDC: 52584-215
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: 52584-215
Labeler Name: General Injectables & Vaccines, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070256
Marketing Category: ANDA
Start Marketing Date: 20100801

Package Information of Naloxone Hydrochloride

Package NDC: 52584-215-01
Package Description: 1 VIAL, SINGLE-DOSE in 1 BAG (52584-215-01) > 1 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Naloxone Hydrochloride

NDC Code 52584-215-01
Proprietary Name Naloxone Hydrochloride
Package Description 1 VIAL, SINGLE-DOSE in 1 BAG (52584-215-01) > 1 mL in 1 VIAL, SINGLE-DOSE
Product NDC 52584-215
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naloxone Hydrochloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 20100801
Marketing Category Name ANDA
Labeler Name General Injectables & Vaccines, 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


General Information