NDC codes

FDA NDC Directory
Product NDC (as listed)0054-0327Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00054-0327Add 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
0054-0327-56000540327561 POUCH in 1 CARTON (0054-0327-56) / 1 INHALER in 1 POUCH / 60 POWDER in 1 INHALERMarketed from Dec 17, 2020

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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)
fluticasone propionate and salmeterol
Generic name (nonproprietary)
fluticasone propionate and salmeterol
Active ingredients
Salmeterol xinafoate — 50 ug/1Fluticasone propionate — 250 ug/1
Dosage form
Powder
Route
Respiratory (Inhalation)
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 203433
Marketing start
Listing expires
Other FDA classes
Adrenergic beta2-Agonists (Mechanism)Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 0054-0327_e2206df8-d8d5-4bef-beff-e70c42419d01SPL ID e2206df8-d8d5-4bef-beff-e70c42419d01SPL set ID f9fcfc90-3677-4a9b-900e-44417d50d507RxCUI 896184, 896209, 896228UNII 6EW8Q962A5, O2GMZ0LF5W
Pharmacologic class
Corticosteroid; 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

N400054032756 followed by a unit qualifier and the quantity

Package 00054-0327-56. 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)

Fluticasone propionate and salmeterol inhalation powder is a combination product containing a corticosteroid and a long-acting beta 2 -adrenergic agonist (LABA) indicated for: • Twice-daily treatment of asthma in patients aged 4 years and older. ( 1.1 ) • Maintenance treatment of airflow obstruction and reducing exacerbations in patients with chronic obstructive pulmonary disease (COPD). ( 1.2 ) Important Limitation of Use: Not indicated for relief of acute bronchospasm. ( 1.1 , 1.2 ) 1.1 Treatment of Asthma Fluticasone propionate and salmeterol inhalation powder is indicated for the twice-daily treatment of asthma in patients aged 4 years and older. Fluticasone propionate and salmeterol inh…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 203433

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

FDA NDC Directory listings under ANDA 203433
ProductStrengthForm · routeLabelerProduct NDC
fluticasone propionate and salmeterolSalmeterol xinafoate 50 ug/1; Fluticasone propionate 100 ug/1PowderRespiratory (Inhalation)REMEDYREPACK INC.70518-4406
fluticasone propionate and salmeterolSalmeterol xinafoate 50 ug/1; Fluticasone propionate 250 ug/1PowderRespiratory (Inhalation)Preferred Pharmaceuticals Inc.68788-8453
fluticasone propionate and salmeterolSalmeterol xinafoate 50 ug/1; Fluticasone propionate 250 ug/1PowderRespiratory (Inhalation)REMEDYREPACK INC.70518-3968
fluticasone propionate and salmeterolSalmeterol xinafoate 50 ug/1; Fluticasone propionate 500 ug/1PowderRespiratory (Inhalation)Hikma Pharmaceuticals USA Inc.0054-0328
fluticasone propionate and salmeterolSalmeterol xinafoate 50 ug/1; Fluticasone propionate 100 ug/1PowderRespiratory (Inhalation)Hikma Pharmaceuticals USA Inc.0054-0326
fluticasone propionate and salmeterolSalmeterol xinafoate 50 ug/1; Fluticasone propionate 100 ug/1PowderRespiratory (Inhalation)Preferred Pharmaceuticals Inc.68788-8704

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fluticasone propionate and salmeterol NDC 0054-0327 | Med-Code