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United States · US · US:68462-531_15a31bdf-5162-42bd-a3d5-7e21bac5f49f
Desoximetasone
Orange BookUNIISPLATC D07AC03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerGlenmark Pharmaceuticals Inc., USA
CountryUS (United States)
ATC codeD07AC03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11684625311715 g in 1 TUBE (68462-531-17)
- ndc11684625316560 g in 1 TUBE (68462-531-65)
Annotations
UNII (FDA Substance ID)
4E07GXB7AU
DESOXIMETASONE
RxCUI 3255
Orange Book
A202838
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": "68462-531_15a31bdf-5162-42bd-a3d5-7e21bac5f49f",
"productndc": "68462-531",
"dosage_form": "OINTMENT",
"orange_book": {
"appl_no": "202838",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "0.25%",
"product_no": "001",
"approval_date": "Sep 20, 2013"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "DESOXIMETASONE",
"proprietary_name": "Desoximetasone",
"active_ingred_unit": "mg/g",
"application_number": "ANDA202838",
"marketing_category": "ANDA",
"nonproprietary_name": "Desoximetasone",
"start_marketing_date": "20130920",
"active_numerator_strength": "2.5"
}Related drugs
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