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SEREVENT

NDA · New Drug Application · Sponsor: GLAXOSMITHKLINE · Approved 1997-09-19

Drug application

FDA Application #
NDA020692
Application type
New Drug Application
Brand name
SEREVENT
Generic name
SALMETEROL XINAFOATE
Active ingredients
SALMETEROL XINAFOATE
Dosage form
POWDER
Route
INHALATION
Marketing status
Prescription
Sponsor
GLAXOSMITHKLINE
Manufacturer
GlaxoSmithKline LLC
First approval
1997-09-19

Source

Authoritative
Drugs@FDA application overview
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