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United States · US · US:51672-1316_3c44a51b-8abe-ceae-e063-6294a90a482c
Alclometasone Dipropionate
Orange BookUNIISPLATC D07AB10
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSun Pharmaceutical Industries, Inc.
CountryUS (United States)
ATC codeD07AB10
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc1151672131611 TUBE in 1 CARTON (51672-1316-1) / 15 g in 1 TUBE
- ndc1151672131631 TUBE in 1 CARTON (51672-1316-3) / 60 g in 1 TUBE
- ndc1151672131655 g in 1 TUBE (51672-1316-5)
- ndc1151672131661 TUBE in 1 CARTON (51672-1316-6) / 45 g in 1 TUBE
Annotations
UNII (FDA Substance ID)
S56PQL4N1V
ALCLOMETASONE DIPROPIONATE
RxCUI 17268
Orange Book
A076730
AB
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": "51672-1316_3c44a51b-8abe-ceae-e063-6294a90a482c",
"productndc": "51672-1316",
"dosage_form": "OINTMENT",
"orange_book": {
"appl_no": "076730",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "0.05%",
"product_no": "001",
"approval_date": "Jul 29, 2004"
}
],
"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": "ANDA076730",
"marketing_category": "ANDA",
"nonproprietary_name": "Alclometasone dipropionate",
"start_marketing_date": "20040729",
"active_numerator_strength": ".5"
}Related drugs
Other records sharing ATC code D07AB10.
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