imiquimod
Generic: imiquimod
Labeler: oceanside pharmacueticalsDrug Facts
Product Profile
Brand Name
imiquimod
Generic Name
imiquimod
Labeler
oceanside pharmacueticals
Dosage Form
CREAM
Routes
Active Ingredients
imiquimod 37.5 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
68682-272
Product ID
68682-272_36b25854-8ed2-8f45-e063-6294a90a8b46
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA022483
Listing Expiration
2026-12-31
Marketing Start
2018-06-27
Pharmacologic Class
Mechanism of Action
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68682272
Hyphenated Format
68682-272
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
NDA022483 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 37.5 mg/g
Packaging
- 1 BOTTLE, PUMP in 1 CARTON (68682-272-75) / 7.5 g in 1 BOTTLE, PUMP
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "36b25854-8ed2-8f45-e063-6294a90a8b46", "openfda": {"nui": ["N0000009267", "N0000009269", "N0000000157"], "unii": ["P1QW714R7M"], "rxcui": ["967017"], "spl_set_id": ["d86eeb0e-70e0-4c72-aaa3-37daa1d8611e"], "pharm_class_pe": ["Increased Cytokine Activity [PE]", "Increased Cytokine Production [PE]"], "pharm_class_moa": ["Interferon Inducers [MoA]"], "manufacturer_name": ["Oceanside Pharmacueticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PUMP in 1 CARTON (68682-272-75) / 7.5 g in 1 BOTTLE, PUMP", "package_ndc": "68682-272-75", "marketing_start_date": "20180627"}], "brand_name": "Imiquimod", "product_id": "68682-272_36b25854-8ed2-8f45-e063-6294a90a8b46", "dosage_form": "CREAM", "pharm_class": ["Increased Cytokine Activity [PE]", "Increased Cytokine Production [PE]", "Interferon Inducers [MoA]"], "product_ndc": "68682-272", "generic_name": "imiquimod", "labeler_name": "Oceanside Pharmacueticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Imiquimod", "active_ingredients": [{"name": "IMIQUIMOD", "strength": "37.5 mg/g"}], "application_number": "NDA022483", "marketing_category": "NDA", "marketing_start_date": "20180627", "listing_expiration_date": "20261231"}