Akten - 17478-792-01 - (lidocaine hydrochloride)

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Drug Information of Akten

Product NDC: 17478-792
Proprietary Name: Akten
Non Proprietary Name: lidocaine hydrochloride
Active Ingredient(s): 35    mg/mL & nbsp;   lidocaine hydrochloride
Administration Route(s): OPHTHALMIC
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Akten

Product NDC: 17478-792
Labeler Name: Akorn, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022221
Marketing Category: NDA
Start Marketing Date: 20081008

Package Information of Akten

Package NDC: 17478-792-01
Package Description: 1 TUBE in 1 CARTON (17478-792-01) > 1 mL in 1 TUBE

NDC Information of Akten

NDC Code 17478-792-01
Proprietary Name Akten
Package Description 1 TUBE in 1 CARTON (17478-792-01) > 1 mL in 1 TUBE
Product NDC 17478-792
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lidocaine hydrochloride
Dosage Form Name GEL
Route Name OPHTHALMIC
Start Marketing Date 20081008
Marketing Category Name NDA
Labeler Name Akorn, Inc.
Substance Name LIDOCAINE HYDROCHLORIDE
Strength Number 35
Strength Unit mg/mL
Pharmaceutical Classes Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE]

Complete Information of Akten


General Information