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United States · US · US:57237-157_641cf1c4-6d24-4ad7-b85a-b2ddbb9263c4
Repaglinide
Orange BookUNIISPLATC A10BX02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerRising Pharma Holdings, Inc.
CountryUS (United States)
ATC codeA10BX02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc115723715701100 TABLET in 1 BOTTLE (57237-157-01)
- ndc115723715705500 TABLET in 1 BOTTLE (57237-157-05)
Annotations
UNII (FDA Substance ID)
668Z8C33LU
REPAGLINIDE
RxCUI 73044
Orange Book
A203820
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "668Z8C33LU",
"rxcui": "73044",
"inchikey": "FAEKWTJYAYMJKF-QHCPKHFHSA-N",
"display_name": "REPAGLINIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"6ae28683-28cc-408e-90f9-6a3dddfc668d": {
"match": "brand_token",
"title": "REPAGLINIDE TABLET [BRYANT RANCH PREPACK]",
"spl_version": "100",
"published_date": "2025-11-17"
}
},
"productid": "57237-157_641cf1c4-6d24-4ad7-b85a-b2ddbb9263c4",
"productndc": "57237-157",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "203820",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "0.5MG",
"product_no": "001",
"approval_date": "Jan 22, 2014"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "1MG",
"product_no": "002",
"approval_date": "Jan 22, 2014"
},
{
"rs": true,
"rld": false,
"te_code": "AB",
"strength": "2MG",
"product_no": "003",
"approval_date": "Jan 22, 2014"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "REPAGLINIDE",
"proprietary_name": "Repaglinide",
"active_ingred_unit": "mg/1",
"application_number": "ANDA203820",
"marketing_category": "ANDA",
"nonproprietary_name": "Repaglinide",
"start_marketing_date": "20140122",
"active_numerator_strength": ".5"
}Related drugs
Other records sharing ATC code A10BX02.
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