Xylocaine - 63323-495-07 - (LIDOCAINE HYDROCHLORIDE)

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Drug Information of Xylocaine

Product NDC: 63323-495
Proprietary Name: Xylocaine
Non Proprietary Name: LIDOCAINE HYDROCHLORIDE
Active Ingredient(s): 20    mg/mL & nbsp;   LIDOCAINE HYDROCHLORIDE
Administration Route(s): EPIDURAL; INFILTRATION; INTRACAUDAL; PERINEURAL
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Xylocaine

Product NDC: 63323-495
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA006488
Marketing Category: NDA
Start Marketing Date: 20100812

Package Information of Xylocaine

Package NDC: 63323-495-07
Package Description: 25 VIAL, SINGLE-DOSE in 1 CARTON (63323-495-07) > 5 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Xylocaine

NDC Code 63323-495-07
Proprietary Name Xylocaine
Package Description 25 VIAL, SINGLE-DOSE in 1 CARTON (63323-495-07) > 5 mL in 1 VIAL, SINGLE-DOSE
Product NDC 63323-495
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LIDOCAINE HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name EPIDURAL; INFILTRATION; INTRACAUDAL; PERINEURAL
Start Marketing Date 20100812
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


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