NDC codes

FDA NDC Directory
Product NDC (as listed)50090-8016Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-8016Add 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
50090-8016-0500908016005 PACKAGE in 1 CARTON (50090-8016-0) / 4 POWDER in 1 PACKAGEMarketed from Jul 16, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
Relenza
Generic name (nonproprietary)
zanamivir
Active ingredients
Zanamivir — 5 mg/1
Dosage form
Powder
Route
Respiratory (Inhalation)
Labeler
A-S Medication SolutionsNDC labeler code 50090
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 021036
Marketing start
Listing expires
Other FDA classes
Neuraminidase Inhibitors (Mechanism)
Identifiers
Product ID 50090-8016_571ce280-f506-436c-b378-d570cceae236SPL ID 571ce280-f506-436c-b378-d570cceae236SPL set ID b4e68930-4e6d-4d27-b1f0-abf60d12e28dRxCUI 759471, 759473UNII L6O3XI777I
Pharmacologic class
Neuraminidase Inhibitor

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

N450090801600 followed by a unit qualifier and the quantity

Package 50090-8016-00. 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 .

Indications (excerpt from the label)

RELENZA, an influenza virus neuraminidase inhibitor (NAI), is indicated for: Treatment of acute, uncomplicated influenza type A and B infections in patients aged 7 years and older who have been symptomatic for no more than 2 days. ( 1.1 ) Prophylaxis of influenza in patients aged 5 years and older. ( 1.2 ) Important Limitations of Use: Not recommended for treatment or prophylaxis of influenza in: • Individuals with underlying airways disease. ( 5.1 ) Not proven effective for: • Treatment in individuals with underlying airways disease. ( 1.3 ) • Prophylaxis in nursing home residents. ( 1.3 ) Not a substitute for annual influenza vaccination. ( 1.3 ) Consider available information on influenza…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 50090-8016

What is NDC 50090-8016?
50090-8016 is the product NDC for Relenza (zanamivir), Zanamivir 5 mg/1 powder, listed with the FDA by A-S Medication Solutions. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Relenza (Zanamivir).
What is the active ingredient?
Zanamivir.
Who is the labeler?
A-S Medication Solutions, NDC labeler code 50090. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Relenza?
1 other product NDC are listed under this name. See all Relenza NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Relenza NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
RelenzazanamivirZanamivir 5 mg/1PowderRespiratory (Inhalation)GlaxoSmithKline LLC0173-068100173-0681-0100173-0681-22

Other NDCs under NDA 021036

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

FDA NDC Directory listings under NDA 021036
ProductStrengthForm · routeLabelerProduct NDC
RelenzazanamivirZanamivir 5 mg/1PowderRespiratory (Inhalation)GlaxoSmithKline LLC0173-0681

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