Lidocaine - 50383-933-35 - (Lidocaine)

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Drug Information of Lidocaine

Product NDC: 50383-933
Proprietary Name: Lidocaine
Non Proprietary Name: Lidocaine
Active Ingredient(s): 5    g/100g & nbsp;   Lidocaine
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Lidocaine

Product NDC: 50383-933
Labeler Name: Hi-Tech Pharmacal Co., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040911
Marketing Category: ANDA
Start Marketing Date: 20120312

Package Information of Lidocaine

Package NDC: 50383-933-35
Package Description: 1 TUBE in 1 CARTON (50383-933-35) > 35.44 g in 1 TUBE

NDC Information of Lidocaine

NDC Code 50383-933-35
Proprietary Name Lidocaine
Package Description 1 TUBE in 1 CARTON (50383-933-35) > 35.44 g in 1 TUBE
Product NDC 50383-933
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lidocaine
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20120312
Marketing Category Name ANDA
Labeler Name Hi-Tech Pharmacal Co., Inc.
Substance Name LIDOCAINE
Strength Number 5
Strength Unit g/100g
Pharmaceutical Classes Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE]

Complete Information of Lidocaine


General Information