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LIDOCAINE HYDROCHLORIDE - 54868-2064-0 - (LIDOCAINE HYDROCHLORIDE ANHYDROUS)

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Drug Information of LIDOCAINE HYDROCHLORIDE

Product NDC: 54868-2064
Proprietary Name: LIDOCAINE HYDROCHLORIDE
Non Proprietary Name: LIDOCAINE HYDROCHLORIDE ANHYDROUS
Active Ingredient(s): 20    mg/mL & nbsp;   LIDOCAINE HYDROCHLORIDE ANHYDROUS
Administration Route(s): INFILTRATION
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of LIDOCAINE HYDROCHLORIDE

Product NDC: 54868-2064
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088327
Marketing Category: ANDA
Start Marketing Date: 19940823

Package Information of LIDOCAINE HYDROCHLORIDE

Package NDC: 54868-2064-0
Package Description: 1 VIAL, MULTI-DOSE in 1 CELLO PACK (54868-2064-0) > 50 mL in 1 VIAL, MULTI-DOSE

NDC Information of LIDOCAINE HYDROCHLORIDE

NDC Code 54868-2064-0
Proprietary Name LIDOCAINE HYDROCHLORIDE
Package Description 1 VIAL, MULTI-DOSE in 1 CELLO PACK (54868-2064-0) > 50 mL in 1 VIAL, MULTI-DOSE
Product NDC 54868-2064
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LIDOCAINE HYDROCHLORIDE ANHYDROUS
Dosage Form Name INJECTION, SOLUTION
Route Name INFILTRATION
Start Marketing Date 19940823
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name LIDOCAINE HYDROCHLORIDE ANHYDROUS
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 HYDROCHLORIDE


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