NDC 63323-273

Sumatriptan Succinate 6 mg per 0.5 mL injection

On the label: Fresenius Kabi, LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Fresenius Kabi USA, LLCGrand Island, NY, United StatesMakes it and tests it Problems found, fixed voluntarilyOct 13, 2023 · 14 inspections, 2 with FDA action

Product details

Generic drug
Sumatriptan: every company that makes it
Form
injection, subcutaneous
Strength
6 mg per 0.5 mL
Approval
ANDA ANDA079242
On the market since
Apr 12, 2011
Package NDCs
63323-273-01
Official label
DailyMed (National Library of Medicine), updated Apr 12, 2024

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