Imiquimod
These highlights do not include all the information needed to use Imiquimod safely and effectively. See full prescribing information for Imiquimod. Imiquimod Cream, 5% For topical use only Initial U.S. Approval: 1997
Approved
Approval ID
47e471c2-4d26-4393-9f04-297fea8411ac
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jul 12, 2011
Manufacturers
FDA
Taro Pharmaceutical Industries Ltd.
DUNS: 600072078
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Imiquimod
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code52549-4145
Application NumberANDA200173
Product Classification
M
Marketing Category
C73584
G
Generic Name
Imiquimod
Product Specifications
Route of AdministrationTOPICAL
Effective DateJuly 12, 2011
FDA Product Classification
INGREDIENTS (13)
ImiquimodActive
Quantity: 50 mg in 1 g
Code: P1QW714R7M
Classification: ACTIB
benzyl alcoholInactive
Code: LKG8494WBH
Classification: IACT
cetyl alcoholInactive
Code: 936JST6JCN
Classification: IACT
glycerinInactive
Code: PDC6A3C0OX
Classification: IACT
waterInactive
Code: 059QF0KO0R
Classification: IACT
methylparabenInactive
Code: A2I8C7HI9T
Classification: IACT
sorbitan monostearateInactive
Code: NVZ4I0H58X
Classification: IACT
stearyl alcoholInactive
Code: 2KR89I4H1Y
Classification: IACT
petrolatumInactive
Code: 4T6H12BN9U
Classification: IACT
isostearic acidInactive
Code: X33R8U0062
Classification: IACT
polysorbate 60Inactive
Code: CAL22UVI4M
Classification: IACT
propylparabenInactive
Code: Z8IX2SC1OH
Classification: IACT
xanthan gumInactive
Code: TTV12P4NEE
Classification: IACT