Drugplain

SEREVENT DISKUS 50 ug/1

salmeterol xinafoate · POWDER, METERED · GlaxoSmithKline LLC

No Recall History
Plain English

SEREVENT DISKUS is a powder, metered containing salmeterol xinafoate at 50 ug/1, taken oral. Manufactured by GlaxoSmithKline LLC.

Key Facts

Brand Name
SEREVENT DISKUS
Generic Name
salmeterol xinafoate
NDC Code (Product)
0173-0521
Manufacturer
GlaxoSmithKline LLC
Strength
50 ug/1
Dosage Form
POWDER, METERED
Route
ORAL, RESPIRATORY (INHALATION)
Marketing Status
Application #
NDA020692
Marketing Start
11/25/1997

Recall History

No Recall History

Frequently Asked Questions

What is SEREVENT DISKUS used for?

SEREVENT DISKUS contains salmeterol xinafoate. It is a powder, metered taken oral. Consult your doctor for specific uses.

Is SEREVENT DISKUS a controlled substance?

SEREVENT DISKUS is not classified as a controlled substance by the DEA.

What is the generic name for SEREVENT DISKUS?

The generic name for SEREVENT DISKUS is salmeterol xinafoate. There are no other listed brand versions of salmeterol xinafoate.

What is the NDC code for SEREVENT DISKUS 50 ug/1?

The NDC (National Drug Code) for SEREVENT DISKUS 50 ug/1 is 0173-0521, listed by GlaxoSmithKline LLC.

Product NDC

0173-0521

Package NDC

0173-0521-00

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)