Lidocaine
FOR EXTERNAL USE ONLYDO NOT USE IN THE EYESRx Only
Approved
Approval ID
7e81c577-5a08-4c97-93e1-7a05c2f7c237
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 21, 2017
Manufacturers
FDA
Liberty Pharmaceuticals, Inc.
DUNS: 012568840
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Lidocaine
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code0440-9715
Application NumberANDA207810
Product Classification
M
Marketing Category
C73584
G
Generic Name
Lidocaine
Product Specifications
Route of AdministrationTOPICAL
Effective DateSeptember 26, 2017
FDA Product Classification
INGREDIENTS (3)
LIDOCAINEActive
Quantity: 50 mg in 1 g
Code: 98PI200987
Classification: ACTIB
POLYETHYLENE GLYCOL 300Inactive
Code: 5655G9Y8AQ
Classification: IACT
POLYETHYLENE GLYCOL 1450Inactive
Code: OJ4Z5Z32L4
Classification: IACT