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United States · US · US:10135-541_43e0b999-0f40-3c9d-e063-6294a90ae477
Probenecid
Orange BookUNIISPLATC M04AB01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerMarlex Pharmaceuticals Inc
CountryUS (United States)
ATC codeM04AB01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc111013554101100 TABLET, FILM COATED in 1 BOTTLE (10135-541-01)
- ndc1110135541101000 TABLET, FILM COATED in 1 BOTTLE (10135-541-10)
Annotations
UNII (FDA Substance ID)
PO572Z7917
PROBENECID
RxCUI 8698
Orange Book
A080966
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": "10135-541_43e0b999-0f40-3c9d-e063-6294a90ae477",
"productndc": "10135-541",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "080966",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "500MG",
"product_no": "001",
"approval_date": "Approved Prior to Jan 1, 1982"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "PROBENECID",
"proprietary_name": "Probenecid",
"active_ingred_unit": "mg/1",
"application_number": "ANDA080966",
"marketing_category": "ANDA",
"nonproprietary_name": "Probenecid",
"start_marketing_date": "19760729",
"active_numerator_strength": "500"
}Related drugs
Other records sharing ATC code M04AB01.
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