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Lidocaine Hydrochloride - 58980-822-60 - (Lidocaine Hydrochloride)

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Drug Information of Lidocaine Hydrochloride

Product NDC: 58980-822
Proprietary Name: Lidocaine Hydrochloride
Non Proprietary Name: Lidocaine Hydrochloride
Active Ingredient(s): 5.31    mL/177mL & nbsp;   Lidocaine Hydrochloride
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Lidocaine Hydrochloride

Product NDC: 58980-822
Labeler Name: Stratus Pharamceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20120301

Package Information of Lidocaine Hydrochloride

Package NDC: 58980-822-60
Package Description: 1 BOTTLE in 1 BOX (58980-822-60) > 177 mL in 1 BOTTLE

NDC Information of Lidocaine Hydrochloride

NDC Code 58980-822-60
Proprietary Name Lidocaine Hydrochloride
Package Description 1 BOTTLE in 1 BOX (58980-822-60) > 177 mL in 1 BOTTLE
Product NDC 58980-822
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lidocaine Hydrochloride
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20120301
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Stratus Pharamceuticals
Substance Name LIDOCAINE HYDROCHLORIDE
Strength Number 5.31
Strength Unit mL/177mL
Pharmaceutical Classes Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE]

Complete Information of Lidocaine Hydrochloride


General Information