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Lidocaine Hydrochloride - 21695-783-00 - (Lidocaine Hydrochloride)

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Drug Information of Lidocaine Hydrochloride

Product NDC: 21695-783
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: 21695-783
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040014
Marketing Category: ANDA
Start Marketing Date: 19950710

Package Information of Lidocaine Hydrochloride

Package NDC: 21695-783-00
Package Description: 100 mL in 1 BOTTLE, PLASTIC (21695-783-00)

NDC Information of Lidocaine Hydrochloride

NDC Code 21695-783-00
Proprietary Name Lidocaine Hydrochloride
Package Description 100 mL in 1 BOTTLE, PLASTIC (21695-783-00)
Product NDC 21695-783
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lidocaine Hydrochloride
Dosage Form Name SOLUTION
Route Name ORAL; TOPICAL
Start Marketing Date 19950710
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
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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