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United States · US · US:72189-084_2be84443-5bdd-96bd-e063-6294a90a9264
IMIQUIMOD
Orange BookUNIISPLATC D06BB10
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerDIRECT RX
CountryUS (United States)
ATC codeD06BB10
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc117218908424.25 g in 1 PACKET (72189-084-24)
Annotations
UNII (FDA Substance ID)
P1QW714R7M
IMIQUIMOD
RxCUI 59943
Orange Book
A078837
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "P1QW714R7M",
"rxcui": "59943",
"inchikey": "DOUYETYNHWVLEO-UHFFFAOYSA-N",
"display_name": "IMIQUIMOD",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"51913a5a-1cab-4b9e-b2c2-e0174062df73": {
"match": "brand_token",
"title": "IMIQUIMOD CREAM [SUN PHARMACEUTICAL INDUSTRIES, INC.]",
"spl_version": "8",
"published_date": "2026-01-26"
}
},
"productid": "72189-084_2be84443-5bdd-96bd-e063-6294a90a9264",
"productndc": "72189-084",
"dosage_form": "CREAM",
"orange_book": {
"appl_no": "078837",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "5%",
"product_no": "001",
"approval_date": "Sep 7, 2010"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "IMIQUIMOD",
"proprietary_name": "IMIQUIMOD",
"active_ingred_unit": "mg/.25g",
"application_number": "ANDA078837",
"marketing_category": "ANDA",
"nonproprietary_name": "IMIQUIMOD",
"start_marketing_date": "20200323",
"active_numerator_strength": "12.5"
}Related drugs
Other records sharing ATC code D06BB10.
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