Xylocaine - 63323-479-30 - (LIDOCAINE HYDROCHLORIDE)

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Drug Information of Xylocaine

Product NDC: 63323-479
Proprietary Name: Xylocaine
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 Xylocaine

Product NDC: 63323-479
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA008816
Marketing Category: NDA
Start Marketing Date: 20100927

Package Information of Xylocaine

Package NDC: 63323-479-30
Package Description: 1 TUBE in 1 CARTON (63323-479-30) > 30 mL in 1 TUBE

NDC Information of Xylocaine

NDC Code 63323-479-30
Proprietary Name Xylocaine
Package Description 1 TUBE in 1 CARTON (63323-479-30) > 30 mL in 1 TUBE
Product NDC 63323-479
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LIDOCAINE HYDROCHLORIDE
Dosage Form Name JELLY
Route Name TOPICAL
Start Marketing Date 20100927
Marketing Category Name NDA
Labeler Name APP Pharmaceuticals, LLC
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 Xylocaine


General Information