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United States · US · US:68462-299_098145f1-cb92-4222-8069-72fbf92fce9f
Alclometasone Dipropionate
Orange BookUNIISPLATC D07AB10
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerGlenmark Pharmaceuticals Inc., USA
CountryUS (United States)
ATC codeD07AB10
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc11684622991715 g in 1 TUBE (68462-299-17)
- ndc11684622994745 g in 1 TUBE (68462-299-47)
- ndc11684622996560 g in 1 TUBE (68462-299-65)
Annotations
UNII (FDA Substance ID)
S56PQL4N1V
ALCLOMETASONE DIPROPIONATE
RxCUI 17268
Orange Book
A079227
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "S56PQL4N1V",
"rxcui": "17268",
"inchikey": "DJHCCTTVDRAMEH-DUUJBDRPSA-N",
"display_name": "ALCLOMETASONE DIPROPIONATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"3b0dccd6-dee1-49dd-8c6d-82df5c7ee36c": {
"match": "brand_token",
"title": "ALCLOMETASONE DIPROPIONATE OINTMENT [SUN PHARMACEUTICAL INDUSTRIES, INC.]",
"spl_version": "6",
"published_date": "2025-08-15"
}
},
"productid": "68462-299_098145f1-cb92-4222-8069-72fbf92fce9f",
"productndc": "68462-299",
"dosage_form": "OINTMENT",
"orange_book": {
"appl_no": "079227",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "0.05%",
"product_no": "001",
"approval_date": "Jul 30, 2009"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ALCLOMETASONE DIPROPIONATE",
"proprietary_name": "Alclometasone Dipropionate",
"active_ingred_unit": "mg/g",
"application_number": "ANDA079227",
"marketing_category": "ANDA",
"nonproprietary_name": "Alclometasone Dipropionate",
"start_marketing_date": "20090730",
"active_numerator_strength": ".5"
}Related drugs
Other records sharing ATC code D07AB10.
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