LidoLite
LidoLite - Lidocaine Ointment USP 5% DO NOT USE IN THE EYES Rx Only
Approved
Approval ID
101e6544-6f24-4c56-8845-d0dcbcf18b10
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 17, 2023
Manufacturers
FDA
Forreal Pharmaceuticals LLC
DUNS: 118029197
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
lidocaine
PRODUCT DETAILS
NDC Product Code81877-660
Application NumberANDA206498
Marketing CategoryC73584
Route of AdministrationTOPICAL
Effective DateNovember 17, 2023
Generic Namelidocaine
INGREDIENTS (3)
LIDOCAINEActive
Quantity: 50 mg in 1 g
Code: 98PI200987
Classification: ACTIB
POLYETHYLENE GLYCOL 1450Inactive
Code: OJ4Z5Z32L4
Classification: IACT
POLYETHYLENE GLYCOL 300Inactive
Code: 5655G9Y8AQ
Classification: IACT