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United States · US · US:71335-1692_3bd5380a-6de4-47fa-92b1-9c3d3874a1ee

bumetanide

In shortageOrange BookUNIISPLATC C03CA02

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

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeC03CA02
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 6

  • ndc11
    7133516921
    30 TABLET in 1 BOTTLE (71335-1692-1)
  • ndc11
    7133516922
    90 TABLET in 1 BOTTLE (71335-1692-2)
  • ndc11
    7133516923
    28 TABLET in 1 BOTTLE (71335-1692-3)
  • ndc11
    7133516924
    18 TABLET in 1 BOTTLE (71335-1692-4)
  • ndc11
    7133516925
    60 TABLET in 1 BOTTLE (71335-1692-5)
  • ndc11
    7133516926
    100 TABLET in 1 BOTTLE (71335-1692-6)

Annotations

UNII (FDA Substance ID)
0Y2S3XUQ5H
BUMETANIDE
RxCUI 1808
Orange Book
A202900
ABABAB
DailyMed SPL labels
1 version tracked
FDA shortage
Currently in shortage
Bumetanide Injection
Raw payload (JSON)
{
  "unii": {
    "unii": "0Y2S3XUQ5H",
    "rxcui": "1808",
    "inchikey": "MAEIEVLCKWDQJH-UHFFFAOYSA-N",
    "display_name": "BUMETANIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "551918e1-96c4-453a-870c-61b282882206": {
      "match": "brand_token",
      "title": "BUMETANIDE TABLET [NORTHSTAR RX LLC]",
      "spl_version": "1",
      "published_date": "2026-06-02"
    }
  },
  "productid": "71335-1692_3bd5380a-6de4-47fa-92b1-9c3d3874a1ee",
  "productndc": "71335-1692",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "202900",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "0.5MG",
        "product_no": "001",
        "approval_date": "Apr 30, 2018"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "1MG",
        "product_no": "002",
        "approval_date": "Apr 30, 2018"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "2MG",
        "product_no": "003",
        "approval_date": "Apr 30, 2018"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "BUMETANIDE",
  "shortage_reason": "Bumetanide Injection",
  "shortage_status": "current",
  "proprietary_name": "bumetanide",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA202900",
  "marketing_category": "ANDA",
  "nonproprietary_name": "bumetanide",
  "start_marketing_date": "20180501",
  "active_numerator_strength": "1"
}

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