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Lidocaine Hydrochloride - 0548-3012-00 - (Lidocaine Hydrochloride)

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Drug Information of Lidocaine Hydrochloride

Product NDC: 0548-3012
Proprietary Name: Lidocaine Hydrochloride
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 Lidocaine Hydrochloride

Product NDC: 0548-3012
Labeler Name: Amphastar Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA086283
Marketing Category: ANDA
Start Marketing Date: 19790807

Package Information of Lidocaine Hydrochloride

Package NDC: 0548-3012-00
Package Description: 25 VIAL, SINGLE-USE in 1 BOX (0548-3012-00) > 5 mL in 1 VIAL, SINGLE-USE

NDC Information of Lidocaine Hydrochloride

NDC Code 0548-3012-00
Proprietary Name Lidocaine Hydrochloride
Package Description 25 VIAL, SINGLE-USE in 1 BOX (0548-3012-00) > 5 mL in 1 VIAL, SINGLE-USE
Product NDC 0548-3012
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lidocaine Hydrochloride
Dosage Form Name JELLY
Route Name TOPICAL
Start Marketing Date 19790807
Marketing Category Name ANDA
Labeler Name Amphastar Pharmaceuticals, Inc.
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 Hydrochloride


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