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United States · US · US:51672-1261_38f63e0c-c4d2-523e-e063-6394a90a0272
Desoximetasone
Orange BookUNIISPLATC D07AC03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSun Pharmaceutical Industries, Inc.
CountryUS (United States)
ATC codeD07AC03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1151672126111 TUBE in 1 CARTON (51672-1261-1) / 15 g in 1 TUBE
- ndc1151672126121 TUBE in 1 CARTON (51672-1261-2) / 30 g in 1 TUBE
- ndc1151672126131 TUBE in 1 CARTON (51672-1261-3) / 60 g in 1 TUBE
Annotations
UNII (FDA Substance ID)
4E07GXB7AU
DESOXIMETASONE
RxCUI 3255
Orange Book
A074904
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "4E07GXB7AU",
"rxcui": "3255",
"inchikey": "VWVSBHGCDBMOOT-IIEHVVJPSA-N",
"display_name": "DESOXIMETASONE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"827aee22-cf48-477c-8791-c74f16da954d": {
"match": "brand_token",
"title": "DESOXIMETASONE CREAM [SAPTALIS PHARMACEUTICALS, LLC.]",
"spl_version": "2",
"published_date": "2026-05-13"
}
},
"productid": "51672-1261_38f63e0c-c4d2-523e-e063-6394a90a0272",
"productndc": "51672-1261",
"dosage_form": "GEL",
"orange_book": {
"appl_no": "074904",
"products": [
{
"rs": true,
"rld": false,
"te_code": "AB",
"strength": "0.05%",
"product_no": "001",
"approval_date": "Jul 14, 1998"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "DESOXIMETASONE",
"proprietary_name": "Desoximetasone",
"active_ingred_unit": "mg/g",
"application_number": "ANDA074904",
"marketing_category": "ANDA",
"nonproprietary_name": "Desoximetasone",
"start_marketing_date": "19980714",
"active_numerator_strength": ".5"
}Related drugs
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