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United States · US · US:70518-4649_5098c53d-d892-0c71-e063-6394a90a9d27
Probenecid
Orange BookUNIISPLATC M04AB01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerREMEDYREPACK INC.
CountryUS (United States)
ATC codeM04AB01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11705184649050 POUCH in 1 BOX (70518-4649-0) / 1 TABLET in 1 POUCH (70518-4649-1)
Annotations
UNII (FDA Substance ID)
PO572Z7917
PROBENECID
RxCUI 8698
Orange Book
A217020
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "PO572Z7917",
"rxcui": "8698",
"inchikey": "DBABZHXKTCFAPX-UHFFFAOYSA-N",
"display_name": "PROBENECID",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"65b4888c-d49a-433f-9bfd-17880ae40069": {
"match": "brand_token",
"title": "PROBENECID TABLET [REMEDYREPACK INC.]",
"spl_version": "1",
"published_date": "2026-04-30"
}
},
"productid": "70518-4649_5098c53d-d892-0c71-e063-6394a90a9d27",
"productndc": "70518-4649",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "217020",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "500MG",
"product_no": "001",
"approval_date": "Nov 20, 2023"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "PROBENECID",
"proprietary_name": "Probenecid",
"active_ingred_unit": "mg/1",
"application_number": "ANDA217020",
"marketing_category": "ANDA",
"nonproprietary_name": "Probenecid",
"start_marketing_date": "20260428",
"active_numerator_strength": "500"
}Related drugs
Other records sharing ATC code M04AB01.
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