Lidocaine Hydrochloride
LIDOCAINE HYDROCHLORIDE INJECTION, USP
Approved
Approval ID
f98b8ed2-5faa-d998-e053-6394a90ac71d
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Apr 17, 2023
Manufacturers
FDA
Medical Purchasing Solutions, LLC
DUNS: 601458529
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
LIDOCAINE HYDROCHLORIDE
PRODUCT DETAILS
NDC Product Code71872-7301
Application NumberANDA083158
Marketing CategoryC73584
Route of AdministrationINTRAVENOUS
Effective DateApril 17, 2023
Generic NameLIDOCAINE HYDROCHLORIDE
INGREDIENTS (4)
HYDROCHLORIC ACIDInactive
Code: QTT17582CB
Classification: IACT
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: IACT
LIDOCAINE HYDROCHLORIDEActive
Quantity: 20 mg in 1 mL
Code: V13007Z41A
Classification: ACTIR