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Lidocaine Hydrochloride - 13925-159-03 - (Lidocaine Hydrochloride)

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Drug Information of Lidocaine Hydrochloride

Product NDC: 13925-159
Proprietary Name: Lidocaine Hydrochloride
Non Proprietary Name: Lidocaine Hydrochloride
Active Ingredient(s): 30    mg/g & nbsp;   Lidocaine Hydrochloride
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Lidocaine Hydrochloride

Product NDC: 13925-159
Labeler Name: Seton Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20110620

Package Information of Lidocaine Hydrochloride

Package NDC: 13925-159-03
Package Description: 1 TUBE in 1 CARTON (13925-159-03) > 85 g in 1 TUBE

NDC Information of Lidocaine Hydrochloride

NDC Code 13925-159-03
Proprietary Name Lidocaine Hydrochloride
Package Description 1 TUBE in 1 CARTON (13925-159-03) > 85 g in 1 TUBE
Product NDC 13925-159
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lidocaine Hydrochloride
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20110620
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Seton Pharmaceuticals
Substance Name LIDOCAINE HYDROCHLORIDE
Strength Number 30
Strength Unit mg/g
Pharmaceutical Classes Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE]

Complete Information of Lidocaine Hydrochloride


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