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United States Β· US Β· US:47918-880_49f26445-3b5b-9c07-e063-6294a90a21a6

AFREZZA

SPL

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

Identification

ManufacturerMannkind Corporation
CountryUS (United States)
ATC codeβ€”
Dispensingβ€”
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs Β· 1

  • ndc11
    4791888018
    1 KIT in 1 CARTON (47918-880-18) * 3 POUCH in 1 PACKAGE, COMBINATION / 2 BLISTER PACK in 1 POUCH / 15 CARTRIDGE in 1 BLISTER PACK / 1 POWDER, METERED in 1 CARTRIDGE * 3 POUCH in 1 PACKAGE, COMBINATION / 2 BLISTER PACK in 1 POUCH / 15 CARTRIDGE in 1 BLISTER PACK / 1 POWDER, METERED in 1 CARTRIDGE

Annotations

DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "route": "RESPIRATORY (INHALATION)",
  "spl_meta": {
    "29f4637b-e204-425b-b89c-7238008d8c10": {
      "match": "brand_token",
      "title": "AFREZZA (INSULIN HUMAN) POWDER, METERED AFREZZA (INSULIN HUMAN) KIT AFREZZA (INSULIN HUMAN) KIT [MANNKIND CORPORATION]",
      "spl_version": "16",
      "published_date": "2026-02-06"
    }
  },
  "productid": "47918-880_49f26445-3b5b-9c07-e063-6294a90a21a6",
  "productndc": "47918-880",
  "dosage_form": "KIT",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": null,
  "proprietary_name": "AFREZZA",
  "active_ingred_unit": null,
  "application_number": "BLA022472",
  "marketing_category": "BLA",
  "nonproprietary_name": "INSULIN HUMAN",
  "start_marketing_date": "20160701",
  "active_numerator_strength": null
}

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