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United States · US · US:63629-4968_e3247459-31c2-48a5-959e-d3ec3d92be66

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
    6362949681
    30 TABLET in 1 BOTTLE (63629-4968-1)
  • ndc11
    6362949682
    90 TABLET in 1 BOTTLE (63629-4968-2)
  • ndc11
    6362949683
    28 TABLET in 1 BOTTLE (63629-4968-3)
  • ndc11
    6362949684
    18 TABLET in 1 BOTTLE (63629-4968-4)
  • ndc11
    6362949685
    60 TABLET in 1 BOTTLE (63629-4968-5)
  • ndc11
    6362949686
    100 TABLET in 1 BOTTLE (63629-4968-6)

Annotations

UNII (FDA Substance ID)
0Y2S3XUQ5H
BUMETANIDE
RxCUI 1808
Orange Book
A074700
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": "63629-4968_e3247459-31c2-48a5-959e-d3ec3d92be66",
  "productndc": "63629-4968",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "074700",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "0.5MG",
        "product_no": "001",
        "approval_date": "Nov 21, 1996"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "1MG",
        "product_no": "002",
        "approval_date": "Nov 21, 1996"
      },
      {
        "rs": true,
        "rld": false,
        "te_code": "AB",
        "strength": "2MG",
        "product_no": "003",
        "approval_date": "Nov 21, 1996"
      }
    ],
    "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": "ANDA074700",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Bumetanide",
  "start_marketing_date": "19961121",
  "active_numerator_strength": "1"
}

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