NDC 68382-922

Eletriptan hydrobromide 20 mg tablet, film coated

On the label: Zydus Pharmaceuticals (USA) Inc..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Zydus Lifesciences LimitedAhmedabad, IndiaMakes it and tests it Problems found, fixed voluntarilyMar 24, 2023 · 5 inspections

Product details

Generic drug
Eletriptan: every company that makes it
Form
tablet, film coated, oral
Strength
20 mg
Approval
ANDA ANDA206409
On the market since
Jul 12, 2017
Package NDCs
68382-922-06 68382-922-10 68382-922-30 68382-922-77 68382-922-86
Official label
DailyMed (National Library of Medicine), updated Sep 18, 2023

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