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United States · US · US:62332-406_afb792df-ffe3-4c77-a9dc-5eb831b2401b
Silodosin
Orange BookUNIISPLATC G04CA04
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAlembic Pharmaceuticals Inc.
CountryUS (United States)
ATC codeG04CA04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc11623324063030 CAPSULE in 1 BOTTLE (62332-406-30)
- ndc11623324069090 CAPSULE in 1 BOTTLE (62332-406-90)
- ndc1162332406911000 CAPSULE in 1 BOTTLE (62332-406-91)
Annotations
UNII (FDA Substance ID)
CUZ39LUY82
SILODOSIN
RxCUI 720825
Orange Book
A211731
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "CUZ39LUY82",
"rxcui": "720825",
"inchikey": "PNCPYILNMDWPEY-QGZVFWFLSA-N",
"display_name": "SILODOSIN",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"43f83422-680f-411e-bbc3-2b092e64a017": {
"match": "brand_token",
"title": "SILODOSIN CAPSULE [CREEKWOOD PHARMACEUTICALS LLC]",
"spl_version": "4",
"published_date": "2026-05-11"
}
},
"productid": "62332-406_afb792df-ffe3-4c77-a9dc-5eb831b2401b",
"productndc": "62332-406",
"dosage_form": "CAPSULE",
"orange_book": {
"appl_no": "211731",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "4MG",
"product_no": "001",
"approval_date": "Nov 22, 2019"
},
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "8MG",
"product_no": "002",
"approval_date": "Nov 22, 2019"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "SILODOSIN",
"proprietary_name": "Silodosin",
"active_ingred_unit": "mg/1",
"application_number": "ANDA211731",
"marketing_category": "ANDA",
"nonproprietary_name": "Silodosin",
"start_marketing_date": "20191125",
"active_numerator_strength": "8"
}Related drugs
Other records sharing ATC code G04CA04.
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