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United States · US · US:0591-5347_8319745d-3201-48c6-b1eb-9ff32e930872
Probenecid
Orange BookUNIISPLATC M04AB01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerActavis Pharma, Inc.
CountryUS (United States)
ATC codeM04AB01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc110591534701100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-5347-01)
- ndc1105915347101000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-5347-10)
Annotations
UNII (FDA Substance ID)
PO572Z7917
PROBENECID
RxCUI 8698
Orange Book
A084442
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": "0591-5347_8319745d-3201-48c6-b1eb-9ff32e930872",
"productndc": "0591-5347",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "084442",
"products": [
{
"rs": true,
"rld": false,
"te_code": "AB",
"strength": "500MG",
"product_no": "004",
"approval_date": "Mar 29, 1983"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "PROBENECID",
"proprietary_name": "Probenecid",
"active_ingred_unit": "mg/1",
"application_number": "ANDA084442",
"marketing_category": "ANDA",
"nonproprietary_name": "Probenecid",
"start_marketing_date": "19830701",
"active_numerator_strength": "500"
}Related drugs
Other records sharing ATC code M04AB01.
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