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United States · US · US:51672-4060_31e404cb-aac7-730b-e063-6394a90afc03
Amcinonide
Orange BookUNIISPLATC D07AC11
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSun Pharmaceutical Industries, Inc.
CountryUS (United States)
ATC codeD07AC11
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1151672406011 TUBE in 1 CARTON (51672-4060-1) / 15 g in 1 TUBE
- ndc1151672406021 TUBE in 1 CARTON (51672-4060-2) / 30 g in 1 TUBE
- ndc1151672406031 TUBE in 1 CARTON (51672-4060-3) / 60 g in 1 TUBE
Annotations
UNII (FDA Substance ID)
423W026MA9
AMCINONIDE
RxCUI 17652
Orange Book
A076367
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "423W026MA9",
"rxcui": "17652",
"inchikey": "ILKJAFIWWBXGDU-MOGDOJJUSA-N",
"display_name": "AMCINONIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"83da75e7-e182-4a6c-ac0f-50d99971ebde": {
"match": "brand_token",
"title": "AMCINONIDE OINTMENT [AYURAX, LLC]",
"spl_version": "3",
"published_date": "2025-11-17"
}
},
"productid": "51672-4060_31e404cb-aac7-730b-e063-6394a90afc03",
"productndc": "51672-4060",
"dosage_form": "OINTMENT",
"orange_book": {
"appl_no": "076367",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "0.1%",
"product_no": "001",
"approval_date": "Mar 19, 2003"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "AMCINONIDE",
"proprietary_name": "Amcinonide",
"active_ingred_unit": "mg/g",
"application_number": "ANDA076367",
"marketing_category": "ANDA",
"nonproprietary_name": "Amcinonide",
"start_marketing_date": "20030319",
"active_numerator_strength": "1"
}Related drugs
Other records sharing ATC code D07AC11.
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