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United States · US · US:51672-1295_39095d21-70bb-6f1d-e063-6394a90a9b9d
Diflorasone Diacetate
Orange BookUNIISPLATC D07AC10
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSun Pharmaceutical Industries, Inc.
CountryUS (United States)
ATC codeD07AC10
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1151672129511 TUBE in 1 CARTON (51672-1295-1) / 15 g in 1 TUBE
- ndc1151672129521 TUBE in 1 CARTON (51672-1295-2) / 30 g in 1 TUBE
- ndc1151672129531 TUBE in 1 CARTON (51672-1295-3) / 60 g in 1 TUBE
Annotations
UNII (FDA Substance ID)
7W2J09SCWX
DIFLORASONE DIACETATE
RxCUI 23033
Orange Book
A075331
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "7W2J09SCWX",
"rxcui": "23033",
"inchikey": "BOBLHFUVNSFZPJ-JOYXJVLSSA-N",
"display_name": "DIFLORASONE DIACETATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"b20c9420-8fb4-4a49-93f0-c0e4074d6d71": {
"match": "brand_token",
"title": "DIFLORASONE DIACETATE CREAM [SUN PHARMACEUTICAL INDUSTRIES, INC.]",
"spl_version": "7",
"published_date": "2025-09-25"
}
},
"productid": "51672-1295_39095d21-70bb-6f1d-e063-6394a90a9b9d",
"productndc": "51672-1295",
"dosage_form": "OINTMENT",
"orange_book": {
"appl_no": "075331",
"products": [
{
"rs": true,
"rld": false,
"te_code": "AB",
"strength": "0.05%",
"product_no": "001",
"approval_date": "May 14, 1999"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "DIFLORASONE DIACETATE",
"proprietary_name": "Diflorasone Diacetate",
"active_ingred_unit": "mg/g",
"application_number": "ANDA075331",
"marketing_category": "ANDA",
"nonproprietary_name": "Diflorasone Diacetate",
"start_marketing_date": "19990514",
"active_numerator_strength": ".5"
}Related drugs
Other records sharing ATC code D07AC10.
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