NDC codes

FDA NDC Directory
Product NDC (as listed)85534-0039Labeler and product segments. Claims need a package NDC.
Product NDC at billing width85534-0039Add 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
85534-0039-0855340039001 CANISTER in 1 CARTON (85534-0039-0) / 200 AEROSOL, METERED in 1 CANISTERMarketed from Jul 3, 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)
Albuterol Sulfate
Generic name (nonproprietary)
albuterol sulfate
Active ingredients
Albuterol sulfate — 90 ug/1
Dosage form
Aerosol, Metered
Route
Respiratory (Inhalation)
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 207085
Marketing start
Listing expires
Other FDA classes
Adrenergic beta2-Agonists (Mechanism)
Identifiers
Product ID 85534-0039_55aecd57-c6eb-8be6-e063-6294a90ad424SPL ID 55aecd57-c6eb-8be6-e063-6294a90ad424SPL set ID b18fad6e-f117-4840-83b7-8c261c646af1RxCUI 2123111UNII 021SEF3731
Pharmacologic class
beta2-Adrenergic Agonist

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

N485534003900 followed by a unit qualifier and the quantity

Package 85534-0039-00. 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)

INDICATIONS AND USAGE Albuterol sulfate inhalation aerosol is indicated in adults and children 4 years of age and older for the treatment or prevention of bronchospasm with reversible obstructive airway disease and for the prevention of exercise-induced bronchospasm.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 207085

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

FDA NDC Directory listings under ANDA 207085
ProductStrengthForm · routeLabelerProduct NDC
Albuterol SulfateAlbuterol sulfate 90 ug/1Aerosol, MeteredRespiratory (Inhalation)Sportpharm LLC85766-020
Albuterol SulfateAlbuterol sulfate 90 ug/1Aerosol, MeteredRespiratory (Inhalation)Preferred Pharmaceuticals Inc.68788-8787
Albuterol SulfateAlbuterol sulfate 90 ug/1Aerosol, MeteredRespiratory (Inhalation)Proficient Rx LP82804-189
Albuterol SulfateAlbuterol sulfate 90 ug/1Aerosol, MeteredRespiratory (Inhalation)Hikma Pharmaceuticals USA Inc.0054-0742
Albuterol SulfateAlbuterol sulfate 90 ug/1Aerosol, MeteredRespiratory (Inhalation)NuCare Pharmaceuticals, Inc.68071-5312
Albuterol SulfateAlbuterol sulfate 90 ug/1Aerosol, MeteredRespiratory (Inhalation)Asclemed USA, Inc.76420-531

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