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United States · US · US:72162-2237_8c261b93-98b4-46ce-a713-11d3b2d7cd13

Probenecid

Orange BookUNIISPLATC M04AB01

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeM04AB01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    7216222371
    100 TABLET, FILM COATED in 1 BOTTLE (72162-2237-1)

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": "72162-2237_8c261b93-98b4-46ce-a713-11d3b2d7cd13",
  "productndc": "72162-2237",
  "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

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