NDC 0143-9638

Sumatriptan 6 mg per 0.5 mL injection

On the label: Hikma Pharmaceuticals USA Inc..

Portugal: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Hikma Farmaceutica (portugal), S.aTerrugem Sintra, PortugalMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyApr 21, 2023 · 9 inspections, 1 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 ANDA200183
On the market since
Sep 16, 2013
Package NDCs
0143-9638-01 0143-9638-05 0143-9638-25
Official label
DailyMed (National Library of Medicine), updated Jan 1, 2021

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