🇺🇸
United States · US · US:59762-0406_6015697f-84b2-49c4-b59a-87956261df64
Risedronate Sodium
Orange BookUNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerMylan Pharmaceuticals, Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1159762040611 TABLET, FILM COATED in 1 DOSE PACK (59762-0406-1)
Annotations
UNII (FDA Substance ID)
HU2YAQ274O
RISEDRONATE SODIUM HEMIPENTAHYDRATE
RxCUI 1356127
Orange Book
N020835
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "HU2YAQ274O",
"rxcui": "1356127",
"inchikey": "HYFDYHPNTXOPPO-UHFFFAOYSA-L",
"display_name": "RISEDRONATE SODIUM HEMIPENTAHYDRATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"c89430be-15f1-4b8b-ab7e-738de716ee7d": {
"match": "brand_token",
"title": "RISEDRONATE SODIUM TABLET, DELAYED RELEASE [MYLAN PHARMACEUTICALS, INC.]",
"spl_version": "7",
"published_date": "2026-05-21"
}
},
"productid": "59762-0406_6015697f-84b2-49c4-b59a-87956261df64",
"productndc": "59762-0406",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "020835",
"products": [
{
"rs": false,
"rld": true,
"te_code": null,
"strength": "30MG",
"product_no": "001",
"approval_date": "Mar 27, 1998"
},
{
"rs": false,
"rld": true,
"te_code": null,
"strength": "5MG",
"product_no": "002",
"approval_date": "Apr 14, 2000"
},
{
"rs": true,
"rld": true,
"te_code": "AB",
"strength": "35MG",
"product_no": "003",
"approval_date": "May 25, 2002"
},
{
"rs": false,
"rld": true,
"te_code": null,
"strength": "75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**",
"product_no": "004",
"approval_date": "Apr 16, 2007"
},
{
"rs": true,
"rld": true,
"te_code": "AB",
"strength": "150MG",
"product_no": "005",
"approval_date": "Apr 22, 2008"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "RISEDRONATE SODIUM HEMIPENTAHYDRATE; RISEDRONATE SODIUM MONOHYDRATE",
"proprietary_name": "Risedronate Sodium",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "NDA020835",
"marketing_category": "NDA AUTHORIZED GENERIC",
"nonproprietary_name": "Risedronate Sodium",
"start_marketing_date": "20080422",
"active_numerator_strength": "129; 21"
}Access this data programmatically
Query Risedronate Sodium and 610,000+ other drug records through a single REST API — with a last_synced_at provenance stamp on every response. Free tier includes 100 requests/day.