Fluticasone Propionate and Salmeterol DISKUS (Fluticasone propionate and salmeterol) NDC 70518-4346

Product information

Brand name (proprietary)

Fluticasone Propionate and Salmeterol DISKUSSuffix: DISKUS

Generic name (nonproprietary)

fluticasone propionate and salmeterol

Active ingredients

Fluticasone propionate — 100 ug/1Salmeterol xinafoate — 50 ug/1

Dosage form

Powder

Route

Respiratory (Inhalation)

Labeler

REMEDYREPACK INC.NDC labeler code 70518

Product type

Prescription drug

Marketing category

NDA authorized genericApplication NDA 021077

Marketing start

May 28, 2025

Listing expires

Dec 31, 2027

Other FDA classes

Adrenergic beta2-Agonists (Mechanism)Corticosteroid Hormone Receptor Agonists (Mechanism)

Identifiers

Product ID 70518-4346_4a03f06c-4519-d9c4-e063-6394a90ab3e0SPL ID 4a03f06c-4519-d9c4-e063-6394a90ab3e0SPL set ID 0a2d1344-f412-41db-9b54-0c92a0743703RxCUI 896184UNII O2GMZ0LF5W, 6EW8Q962A5

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

N470518434600 followed by a unit qualifier and the quantity Copy

Package 70518-4346-00. 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

About NDC 70518-4346

What is NDC 70518-4346?

70518-4346 is the product NDC for Fluticasone Propionate and Salmeterol DISKUS, Fluticasone propionate 100 ug/1; Salmeterol xinafoate 50 ug/1 powder, listed with the FDA by REMEDYREPACK INC.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Fluticasone Propionate and Salmeterol DISKUS (Fluticasone propionate and salmeterol).

What is the active ingredient?

Fluticasone propionate, Salmeterol xinafoate.

Who is the labeler?

REMEDYREPACK INC., NDC labeler code 70518. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Fluticasone Propionate and Salmeterol DISKUS?

11 other product NDCs are listed under this name. See all Fluticasone Propionate and Salmeterol DISKUS NDCs.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory. See Billing references above.

Related NDCs: other Fluticasone Propionate and Salmeterol DISKUS products

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

All 12 Fluticasone Propionate and Salmeterol DISKUS NDCs

Other NDCs under NDA 021077

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