NDC 70518-3968

fluticasone propionate and salmeterol 50 ug / 250 ug powder

On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Hikma Pharmaceuticals USA Inc.'s NDC 0054-0327.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
West-Ward Columbus Inc.Columbus, OH, United StatesMakes it No problems foundApr 30, 2026 · 27 inspections

Product details

Generic drug
Fluticasone and Salmeterol: every company that makes it
Form
powder, respiratory (inhalation)
Strength
50 ug / 250 ug
Approval
ANDA ANDA203433
On the market since
Dec 26, 2023
Package NDCs
70518-3968-0
Official label
DailyMed (National Library of Medicine), updated Jun 11, 2026

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