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Lidocaine Hydrochloride - 68788-9799-1 - (Lidocaine Hydrochloride)

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Drug Information of Lidocaine Hydrochloride

Product NDC: 68788-9799
Proprietary Name: Lidocaine Hydrochloride
Non Proprietary Name: Lidocaine Hydrochloride
Active Ingredient(s): 20    mg/mL & nbsp;   Lidocaine Hydrochloride
Administration Route(s): ORAL; TOPICAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Lidocaine Hydrochloride

Product NDC: 68788-9799
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040014
Marketing Category: ANDA
Start Marketing Date: 20120430

Package Information of Lidocaine Hydrochloride

Package NDC: 68788-9799-1
Package Description: 100 mL in 1 BOTTLE, PLASTIC (68788-9799-1)

NDC Information of Lidocaine Hydrochloride

NDC Code 68788-9799-1
Proprietary Name Lidocaine Hydrochloride
Package Description 100 mL in 1 BOTTLE, PLASTIC (68788-9799-1)
Product NDC 68788-9799
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lidocaine Hydrochloride
Dosage Form Name SOLUTION
Route Name ORAL; TOPICAL
Start Marketing Date 20120430
Marketing Category Name ANDA
Labeler Name Preferred 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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