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United States · US · US:51672-4145_3c178924-2055-ce8d-e063-6294a90a644f
Imiquimod
Orange BookUNIISPLATC D06BB10
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSun Pharmaceutical Industries, Inc.
CountryUS (United States)
ATC codeD06BB10
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11516724145624 PACKET in 1 CARTON (51672-4145-6) / .25 g in 1 PACKET (51672-4145-8)
Annotations
UNII (FDA Substance ID)
P1QW714R7M
IMIQUIMOD
RxCUI 59943
Orange Book
A200173
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": "51672-4145_3c178924-2055-ce8d-e063-6294a90a644f",
"productndc": "51672-4145",
"dosage_form": "CREAM",
"orange_book": {
"appl_no": "200173",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "5%",
"product_no": "001",
"approval_date": "Apr 15, 2011"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "IMIQUIMOD",
"proprietary_name": "Imiquimod",
"active_ingred_unit": "mg/g",
"application_number": "ANDA200173",
"marketing_category": "ANDA",
"nonproprietary_name": "Imiquimod",
"start_marketing_date": "20110415",
"active_numerator_strength": "50"
}Related drugs
Other records sharing ATC code D06BB10.
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