NDC codes

FDA NDC Directory
Product NDC (as listed)71205-441Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71205-0441Add 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
71205-441-85712050441851 INHALER in 1 CARTON (71205-441-85) / 200 AEROSOL, METERED in 1 INHALERMarketed from Apr 1, 2020

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)
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 203760
Marketing start
Listing expires
Other FDA classes
Adrenergic beta2-Agonists (Mechanism)
Identifiers
Product ID 71205-441_539823ee-064c-4094-a74c-b50a07a80bf2SPL ID 539823ee-064c-4094-a74c-b50a07a80bf2SPL set ID 918551c7-c3c1-43bc-b575-b33fdb4e96fcRxCUI 2123072UNII 021SEF3731UPC 0371205441852
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

N471205044185 followed by a unit qualifier and the quantity

Package 71205-0441-85. 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)

Albuterol sulfate inhalation aerosol is a beta 2 -adrenergic agonist indicated for: • Treatment or prevention of bronchospasm in patients 4 years of age and older with reversible obstructive airway disease. (1.1) • Prevention of exercise-induced bronchospasm in patients 4 years of age and older. (1.2) 1.1 Bronchospasm Albuterol sulfate inhalation aerosol is indicated for the treatment or prevention of bronchospasm in patients 4 years of age and older with reversible obstructive airway disease. 1.2 Exercise-Induced Bronchospasm Albuterol sulfate inhalation aerosol is indicated for the prevention of exercise-induced bronchospasm in patients 4 years of age and older.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 203760

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

FDA NDC Directory listings under ANDA 203760
ProductStrengthForm · routeLabelerProduct NDC
Albuterol SulfateAlbuterol sulfate 90 ug/1Aerosol, MeteredRespiratory (Inhalation)HF Acquisition Co LLC, DBA HealthFirst51662-1513
albuterol sulfateAlbuterol sulfate 90 ug/1Aerosol, MeteredRespiratory (Inhalation)Sportpharm LLC85766-055
albuterol sulfateAlbuterol sulfate 90 ug/1Aerosol, MeteredRespiratory (Inhalation)Padagis Israel Pharmaceuticals Ltd45802-088

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