NDC codes

FDA NDC Directory
Product NDC (as listed)47918-904Labeler and product segments. Claims need a package NDC.
Product NDC at billing width47918-0904Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
47918-904-30479180904301 KIT in 1 CARTON (47918-904-30) * 15 CARTRIDGE in 1 BLISTER PACK / 1 POWDER, METERED in 1 CARTRIDGE * 15 CARTRIDGE in 1 BLISTER PACK / 1 POWDER, METERED in 1 CARTRIDGEMarketed from Jun 1, 2025 · Sample package

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Afrezza
Generic name (nonproprietary)
insulin human
Dosage form
Kit
Route
Respiratory (Inhalation)
Product type
Prescription drug
Marketing category
BLA — Biologics License ApplicationApplication BLA 022472
Marketing start
Listing expires
Identifiers
Product ID 47918-904_51ca8d95-025a-6342-e063-6294a90a94eeSPL ID 51ca8d95-025a-6342-e063-6294a90a94eeSPL set ID 29f4637b-e204-425b-b89c-7238008d8c10RxCUI 1543202, 1543207, 1544488, 1544490, 1654910, 1654912, 1798387, 1798388, 1862101, 1862102, 2100028, 2100029, 2715452, 2715453UNII 1Y17CTI5SR

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N447918090430 followed by a unit qualifier and the quantity

Package 47918-0904-30. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective . This label includes a boxed warning.

Indications (excerpt from the label)

AFREZZA ® is indicated to improve glycemic control in adult and pediatric patients 6 years of age and older with diabetes mellitus. AFREZZA ® is a rapid acting inhaled human insulin indicated to improve glycemic control in adult and pediatric patients 6 years of age and older with diabetes mellitus. ( 1 ) Limitations of Use : Not recommended for the treatment of diabetic ketoacidosis (DKA) ( 1 ) Not recommended in patients who smoke or who have recently stopped smoking ( 1 ) Limitations of Use: AFREZZA is not recommended for the treatment of diabetic ketoacidosis (DKA) [see Warnings and Precautions ( 5.6 )] . The safety and effectiveness of AFREZZA in patients who smoke have not been establi

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under BLA 022472

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under BLA 022472
ProductStrengthForm · routeLabelerProduct NDC
Afrezzainsulin humanInsulin human 8 [arb'U]/1Powder, MeteredRespiratory (Inhalation)Mannkind Corporation47918-878
Afrezzainsulin humanInsulin human 4 [arb'U]/1Powder, MeteredRespiratory (Inhalation)Mannkind Corporation47918-874
Afrezzainsulin humanKitRespiratory (Inhalation)Mannkind Corporation47918-902
Afrezzainsulin humanKitRespiratory (Inhalation)Mannkind Corporation47918-880
Afrezzainsulin humanInsulin human 12 [arb'U]/1Powder, MeteredRespiratory (Inhalation)Mannkind Corporation47918-891
Afrezzainsulin humanKitRespiratory (Inhalation)Mannkind Corporation47918-898

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Afrezza (insulin human) NDC 47918-904 | Med-Code