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Lidocaine Hydrochloride - 35356-936-30 - (Lidocaine)

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Drug Information of Lidocaine Hydrochloride

Product NDC: 35356-936
Proprietary Name: Lidocaine Hydrochloride
Non Proprietary Name: Lidocaine
Active Ingredient(s): 30    mg/g & nbsp;   Lidocaine
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Lidocaine Hydrochloride

Product NDC: 35356-936
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20130301

Package Information of Lidocaine Hydrochloride

Package NDC: 35356-936-30
Package Description: 1 TUBE in 1 CARTON (35356-936-30) > 28.5 g in 1 TUBE

NDC Information of Lidocaine Hydrochloride

NDC Code 35356-936-30
Proprietary Name Lidocaine Hydrochloride
Package Description 1 TUBE in 1 CARTON (35356-936-30) > 28.5 g in 1 TUBE
Product NDC 35356-936
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lidocaine
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20130301
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
Substance Name LIDOCAINE
Strength Number 30
Strength Unit mg/g
Pharmaceutical Classes Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE]

Complete Information of Lidocaine Hydrochloride


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