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United States · US · US:71930-010_c304be8d-9fa3-4d89-885e-5a6bf1e80a2b
Alosetron Hydrochloride
Orange BookUNIISPLATC A03AE01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerEywa Pharma Inc
CountryUS (United States)
ATC codeA03AE01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11719300103030 TABLET in 1 BOTTLE (71930-010-30)
Annotations
UNII (FDA Substance ID)
2F5R1A46YW
ALOSETRON HYDROCHLORIDE
RxCUI 85247
Orange Book
A211621
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "2F5R1A46YW",
"rxcui": "85247",
"inchikey": "FNYQZOVOVDSGJH-UHFFFAOYSA-N",
"display_name": "ALOSETRON HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"38f5341f-5ae3-46bf-8bfc-30dff2068477": {
"match": "brand_token",
"title": "ALOSETRON TABLET [BRYANT RANCH PREPACK]",
"spl_version": "103",
"published_date": "2026-04-03"
}
},
"productid": "71930-010_c304be8d-9fa3-4d89-885e-5a6bf1e80a2b",
"productndc": "71930-010",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "211621",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 0.5MG BASE",
"product_no": "001",
"approval_date": "Sep 16, 2019"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 1MG BASE",
"product_no": "002",
"approval_date": "Sep 16, 2019"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ALOSETRON HYDROCHLORIDE",
"proprietary_name": "Alosetron Hydrochloride",
"active_ingred_unit": "mg/1",
"application_number": "ANDA211621",
"marketing_category": "ANDA",
"nonproprietary_name": "Alosetron Hydrochloride",
"start_marketing_date": "20190201",
"active_numerator_strength": ".5"
}Related drugs
Other records sharing ATC code A03AE01.
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