imiquimod

Product NDC

64380-773

11-digit product format

643800773

Labeler code

64380

Product ID

64380-773_cdd54008-c33a-4adb-96a8-65e062a0b0a8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

imiquimod

Dosage form

CREAM

Route

TOPICAL

Labeler

Strides Shasun Limited

Application

ANDA202002

Marketing category

ANDA

Marketing start

2014-06-24

Marketing end

0000-00-00

Substance

IMIQUIMOD

Active strength

50 mg/g

Pharmacologic classes

Increased Cytokine Activity [PE],Increased Cytokine Production [PE],Interferon Inducers [MoA]

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record