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Lidocaine Hydrochloride - 55150-162-05 - (Lidocaine Hydrochloride)

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Drug Information of Lidocaine Hydrochloride

Product NDC: 55150-162
Proprietary Name: Lidocaine Hydrochloride
Non Proprietary Name: Lidocaine Hydrochloride
Active Ingredient(s): 10    mg/mL & nbsp;   Lidocaine Hydrochloride
Administration Route(s): EPIDURAL; INFILTRATION; INTRACAUDAL; PERINEURAL
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Lidocaine Hydrochloride

Product NDC: 55150-162
Labeler Name: AuroMedics Pharma LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA203082
Marketing Category: ANDA
Start Marketing Date: 20130314

Package Information of Lidocaine Hydrochloride

Package NDC: 55150-162-05
Package Description: 10 VIAL, SINGLE-DOSE in 1 CARTON (55150-162-05) > 5 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Lidocaine Hydrochloride

NDC Code 55150-162-05
Proprietary Name Lidocaine Hydrochloride
Package Description 10 VIAL, SINGLE-DOSE in 1 CARTON (55150-162-05) > 5 mL in 1 VIAL, SINGLE-DOSE
Product NDC 55150-162
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lidocaine Hydrochloride
Dosage Form Name INJECTION, SOLUTION
Route Name EPIDURAL; INFILTRATION; INTRACAUDAL; PERINEURAL
Start Marketing Date 20130314
Marketing Category Name ANDA
Labeler Name AuroMedics Pharma LLC
Substance Name LIDOCAINE HYDROCHLORIDE
Strength Number 10
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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