Lidocaine - 63323-202-02 - (LIDOCAINE HYDROCHLORIDE)

Alphabetical Index


Drug Information of Lidocaine

Product NDC: 63323-202
Proprietary Name: Lidocaine
Non Proprietary Name: LIDOCAINE HYDROCHLORIDE
Active Ingredient(s): 20    mg/mL & nbsp;   LIDOCAINE HYDROCHLORIDE
Administration Route(s): INFILTRATION; PERINEURAL
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Lidocaine

Product NDC: 63323-202
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA080404
Marketing Category: ANDA
Start Marketing Date: 20100527

Package Information of Lidocaine

Package NDC: 63323-202-02
Package Description: 25 VIAL in 1 TRAY (63323-202-02) > 2 mL in 1 VIAL

NDC Information of Lidocaine

NDC Code 63323-202-02
Proprietary Name Lidocaine
Package Description 25 VIAL in 1 TRAY (63323-202-02) > 2 mL in 1 VIAL
Product NDC 63323-202
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LIDOCAINE HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INFILTRATION; PERINEURAL
Start Marketing Date 20100527
Marketing Category Name ANDA
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 Lidocaine


General Information