NDC 0527-1859

Sumatriptan 20 mg per 0.1 mL spray

On the label: Lannett Company, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Summit Biosciences Inc.Lexington, KY, United StatesMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyFeb 21, 2025 · 4 inspections

Product details

Generic drug
Sumatriptan: every company that makes it
Form
spray, nasal
Strength
20 mg per 0.1 mL
Approval
ANDA ANDA204841
On the market since
Feb 19, 2016
Package NDCs
0527-1859-43
Official label
DailyMed (National Library of Medicine), updated Jan 4, 2022

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