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United States · US · US:16571-775_f06a97e3-4349-4df3-87de-4479c1ed69bc
Glimepiride
Orange BookUNIISPLATC A10BB12
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerRising Pharma Holdings, Inc.
CountryUS (United States)
ATC codeA10BB12
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc111657177501100 TABLET in 1 BOTTLE (16571-775-01)
- ndc111657177550500 TABLET in 1 BOTTLE (16571-775-50)
Annotations
UNII (FDA Substance ID)
6KY687524K
GLIMEPIRIDE
RxCUI 25789
Orange Book
A202759
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "6KY687524K",
"rxcui": "25789",
"inchikey": "WIGIZIANZCJQQY-RUCARUNLSA-N",
"display_name": "GLIMEPIRIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"9e863f84-d6f2-4d61-8250-774569e84353": {
"match": "brand_token",
"title": "GLIMEPIRIDE TABLET [BRYANT RANCH PREPACK]",
"spl_version": "12",
"published_date": "2026-05-21"
}
},
"productid": "16571-775_f06a97e3-4349-4df3-87de-4479c1ed69bc",
"productndc": "16571-775",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "202759",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "1MG",
"product_no": "001",
"approval_date": "Jun 29, 2012"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "2MG",
"product_no": "002",
"approval_date": "Jun 29, 2012"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "4MG",
"product_no": "003",
"approval_date": "Jun 29, 2012"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "GLIMEPIRIDE",
"proprietary_name": "Glimepiride",
"active_ingred_unit": "mg/1",
"application_number": "ANDA202759",
"marketing_category": "ANDA",
"nonproprietary_name": "Glimepiride",
"start_marketing_date": "20120629",
"active_numerator_strength": "4"
}Related drugs
Other records sharing ATC code A10BB12.
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