Lidocaine
LIDOCAINE OINTMENT USP, 5%
Approved
Approval ID
a1e2c14f-0682-4b19-9159-de0aca1960c6
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 1, 2010
Manufacturers
FDA
Rebel Distributors Corp
DUNS: 118802834
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 Code21695-826
Application NumberANDA080198
Product Classification
M
Marketing Category
C73584
G
Generic Name
Lidocaine
Product Specifications
Route of AdministrationTOPICAL
Effective DateJuly 15, 2009
FDA Product Classification
INGREDIENTS (3)
polyethylene glycol 300Inactive
Code: 5655G9Y8AQ
Classification: IACT
polyethylene glycol 1450Inactive
Code: OJ4Z5Z32L4
Classification: IACT
lidocaineActive
Quantity: 50 mg in 1 g
Code: 98PI200987
Classification: ACTIB