imiquimod

Generic: imiquimod

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name imiquimod
Generic Name imiquimod
Labeler sun pharmaceutical industries, inc.
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

imiquimod 37.5 mg/g

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 51672-4174
Product ID 51672-4174_48e9d045-e9a2-8452-e063-6294a90af1e9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205971
Listing Expiration 2027-12-31
Marketing Start 2021-01-26

Pharmacologic Class

Mechanism of Action
interferon inducers [moa]
Physiologic Effect
increased cytokine activity [pe] increased cytokine production [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516724174
Hyphenated Format 51672-4174

Supplemental Identifiers

RxCUI
967017
UPC
0351672417499
UNII
P1QW714R7M
NUI
N0000009267 N0000009269 N0000000157

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name imiquimod (source: ndc)
Generic Name imiquimod (source: ndc)
Application Number ANDA205971 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 37.5 mg/g
source: ndc
Packaging
  • 28 PACKET in 1 CARTON (51672-4174-6) / .25 g in 1 PACKET (51672-4174-8)
  • 1 BOTTLE, PUMP in 1 CARTON (51672-4174-9) / 7.5 g in 1 BOTTLE, PUMP
source: ndc

Packages (2)

51672-4174-6 28 PACKET in 1 CARTON (51672-4174-6) / .25 g in 1 PACKET (51672-4174-8) 51672-4174-9 1 BOTTLE, PUMP in 1 CARTON (51672-4174-9) / 7.5 g in 1 BOTTLE, PUMP

Ingredients (1)

imiquimod (37.5 mg/g)

Linked Drug Pages (1)

Imiquimod ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "48e9d045-e9a2-8452-e063-6294a90af1e9", "openfda": {"nui": ["N0000009267", "N0000009269", "N0000000157"], "upc": ["0351672417499"], "unii": ["P1QW714R7M"], "rxcui": ["967017"], "spl_set_id": ["51913a5a-1cab-4b9e-b2c2-e0174062df73"], "pharm_class_pe": ["Increased Cytokine Activity [PE]", "Increased Cytokine Production [PE]"], "pharm_class_moa": ["Interferon Inducers [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "28 PACKET in 1 CARTON (51672-4174-6)  / .25 g in 1 PACKET (51672-4174-8)", "package_ndc": "51672-4174-6", "marketing_start_date": "20210126"}, {"sample": false, "description": "1 BOTTLE, PUMP in 1 CARTON (51672-4174-9)  / 7.5 g in 1 BOTTLE, PUMP", "package_ndc": "51672-4174-9", "marketing_start_date": "20211014"}], "brand_name": "Imiquimod", "product_id": "51672-4174_48e9d045-e9a2-8452-e063-6294a90af1e9", "dosage_form": "CREAM", "pharm_class": ["Increased Cytokine Activity [PE]", "Increased Cytokine Production [PE]", "Interferon Inducers [MoA]"], "product_ndc": "51672-4174", "generic_name": "Imiquimod", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Imiquimod", "active_ingredients": [{"name": "IMIQUIMOD", "strength": "37.5 mg/g"}], "application_number": "ANDA205971", "marketing_category": "ANDA", "marketing_start_date": "20210126", "listing_expiration_date": "20271231"}