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Lidocaine Hydrochloride - 50383-781-30 - (Lidocaine Hydrochloride)

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Drug Information of Lidocaine Hydrochloride

Product NDC: 50383-781
Proprietary Name: Lidocaine Hydrochloride
Non Proprietary Name: Lidocaine Hydrochloride
Active Ingredient(s): 20    mg/mL & nbsp;   Lidocaine Hydrochloride
Administration Route(s): TOPICAL
Dosage Form(s): JELLY
Coding System: National Drug Codes(NDC)

Labeler Information of Lidocaine Hydrochloride

Product NDC: 50383-781
Labeler Name: Hi-Tech Pharmacal Co., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040837
Marketing Category: ANDA
Start Marketing Date: 20110323

Package Information of Lidocaine Hydrochloride

Package NDC: 50383-781-30
Package Description: 1 TUBE, WITH APPLICATOR in 1 CARTON (50383-781-30) > 30 mL in 1 TUBE, WITH APPLICATOR

NDC Information of Lidocaine Hydrochloride

NDC Code 50383-781-30
Proprietary Name Lidocaine Hydrochloride
Package Description 1 TUBE, WITH APPLICATOR in 1 CARTON (50383-781-30) > 30 mL in 1 TUBE, WITH APPLICATOR
Product NDC 50383-781
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lidocaine Hydrochloride
Dosage Form Name JELLY
Route Name TOPICAL
Start Marketing Date 20110323
Marketing Category Name ANDA
Labeler Name Hi-Tech Pharmacal Co., 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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