Lidocaine Hydrochloride
LIDOCAINE HYDROCHLORIDE JELLY USP, 2A STERILE, WATER-SOLUBLE, TOPICAL ANESTHETIC
Approved
Approval ID
ddaee8bc-f55c-48b1-9b0e-ad1e2dd15a2c
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 9, 2023
Manufacturers
FDA
Henry Schein, Inc.
DUNS: 012430880
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
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code0404-9899
Application NumberANDA086283
Product Classification
M
Marketing Category
C73584
G
Generic Name
lidocaine hydrochloride
Product Specifications
Route of AdministrationTOPICAL
Effective DateNovember 9, 2023
FDA Product Classification
INGREDIENTS (1)
LIDOCAINE HYDROCHLORIDEActive
Quantity: 20 mg in 1 mL
Code: V13007Z41A
Classification: ACTIR