LumaSon

Orange BookSPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerBRACCO DIAGNOSTICS INC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0270709973
5 KIT in 1 BOX (0270-7099-73) / 1 KIT in 1 KIT * 25 mg in 1 VIAL * 5 mL in 1 SYRINGE

Annotations

Orange Book

N203684

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "route": null,
  "spl_meta": {
    "69822a55-226c-f133-e3b8-2b5826667c5b": {
      "match": "brand_token",
      "title": "LUMASON (SULFUR HEXAFLUORIDE) KIT LUMASON (SULFUR HEXAFLUORIDE) INJECTION, POWDER, LYOPHILIZED, FOR SUSPENSION [BRACCO DIAGNOSTICS INC]",
      "spl_version": "10",
      "published_date": "2025-12-25"
    }
  },
  "productid": "0270-7099_47b0f2df-0b6c-a221-750d-763d5ece665b",
  "productndc": "0270-7099",
  "dosage_form": "KIT",
  "orange_book": {
    "appl_no": "203684",
    "products": [
      {
        "rs": true,
        "rld": true,
        "te_code": null,
        "strength": "60.7MG/25MG",
        "product_no": "001",
        "approval_date": "Oct 15, 2014"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": null,
  "proprietary_name": "LumaSon",
  "active_ingred_unit": null,
  "application_number": "NDA203684",
  "marketing_category": "NDA",
  "nonproprietary_name": "SULFUR HEXAFLUORIDE",
  "start_marketing_date": "20200115",
  "active_numerator_strength": null
}

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