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Lidocaine Hydrochloride - 0548-3390-00 - (Lidocaine Hydrochloride)

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Drug Information of Lidocaine Hydrochloride

Product NDC: 0548-3390
Proprietary Name: Lidocaine Hydrochloride
Non Proprietary Name: Lidocaine Hydrochloride
Active Ingredient(s): 20    mg/mL & nbsp;   Lidocaine Hydrochloride
Administration Route(s): PARENTERAL
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Lidocaine Hydrochloride

Product NDC: 0548-3390
Labeler Name: Amphastar Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA083173
Marketing Category: ANDA
Start Marketing Date: 20010601

Package Information of Lidocaine Hydrochloride

Package NDC: 0548-3390-00
Package Description: 10 SYRINGE in 1 PACKAGE (0548-3390-00) > 5 mL in 1 SYRINGE

NDC Information of Lidocaine Hydrochloride

NDC Code 0548-3390-00
Proprietary Name Lidocaine Hydrochloride
Package Description 10 SYRINGE in 1 PACKAGE (0548-3390-00) > 5 mL in 1 SYRINGE
Product NDC 0548-3390
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lidocaine Hydrochloride
Dosage Form Name INJECTION
Route Name PARENTERAL
Start Marketing Date 20010601
Marketing Category Name ANDA
Labeler Name Amphastar Pharmaceuticals, Inc.
Substance Name LIDOCAINE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/mL
Pharmaceutical Classes Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE]

Complete Information of Lidocaine Hydrochloride


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