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Lidocaine and Prilocaine - 0781-7058-03 - (Lidocaine and Prilocaine)

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Drug Information of Lidocaine and Prilocaine

Product NDC: 0781-7058
Proprietary Name: Lidocaine and Prilocaine
Non Proprietary Name: Lidocaine and Prilocaine
Active Ingredient(s): 25; 25    mg/g; mg/g & nbsp;   Lidocaine and Prilocaine
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Lidocaine and Prilocaine

Product NDC: 0781-7058
Labeler Name: Sandoz Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076320
Marketing Category: ANDA
Start Marketing Date: 20030827

Package Information of Lidocaine and Prilocaine

Package NDC: 0781-7058-03
Package Description: 1 TUBE in 1 CARTON (0781-7058-03) > 30 g in 1 TUBE

NDC Information of Lidocaine and Prilocaine

NDC Code 0781-7058-03
Proprietary Name Lidocaine and Prilocaine
Package Description 1 TUBE in 1 CARTON (0781-7058-03) > 30 g in 1 TUBE
Product NDC 0781-7058
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lidocaine and Prilocaine
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20030827
Marketing Category Name ANDA
Labeler Name Sandoz Inc.
Substance Name LIDOCAINE; PRILOCAINE
Strength Number 25; 25
Strength Unit mg/g; mg/g
Pharmaceutical Classes Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE],Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Local Anesthesia [PE]

Complete Information of Lidocaine and Prilocaine


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