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Lidocaine Hydrochloride - 0093-9200-31 - (Lidocaine Hydrochloride)

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Drug Information of Lidocaine Hydrochloride

Product NDC: 0093-9200
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: 0093-9200
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA081318
Marketing Category: ANDA
Start Marketing Date: 19950101

Package Information of Lidocaine Hydrochloride

Package NDC: 0093-9200-31
Package Description: 30 mL in 1 TUBE, WITH APPLICATOR (0093-9200-31)

NDC Information of Lidocaine Hydrochloride

NDC Code 0093-9200-31
Proprietary Name Lidocaine Hydrochloride
Package Description 30 mL in 1 TUBE, WITH APPLICATOR (0093-9200-31)
Product NDC 0093-9200
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lidocaine Hydrochloride
Dosage Form Name JELLY
Route Name TOPICAL
Start Marketing Date 19950101
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA 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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