Xylocaine - 63323-496-97 - (LIDOCAINE HYDROCHLORIDE)

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Drug Information of Xylocaine

Product NDC: 63323-496
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: 63323-496
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: 63323-496-97
Package Description: 5 BLISTER PACK in 1 BOX (63323-496-97) > 1 AMPULE in 1 BLISTER PACK > 10 mL in 1 AMPULE

NDC Information of Xylocaine

NDC Code 63323-496-97
Proprietary Name Xylocaine
Package Description 5 BLISTER PACK in 1 BOX (63323-496-97) > 1 AMPULE in 1 BLISTER PACK > 10 mL in 1 AMPULE
Product NDC 63323-496
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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