NDC 35356-439

Sumatriptan Succinate 50 mg tablet

On the label: Lake Erie Medical DBA Quality Care Products LLC. It's a repackaged product: Lake Erie Medical DBA Quality Care Products LLC rebottles it from Dr.Reddy's Laboratories Ltd.'s NDC 55111-292.

Where the pills inside were made

Dr. Reddy's Laboratories Limited

Medchal-Malkajgiri, India · makes it and tests it

Problems found, fixed voluntarily Last FDA inspection Oct 27, 2023. 8 inspections on record.

Repackaging site

Product details

Generic drug
Sumatriptan: see every company that makes it
Form
tablet
Strength
50 mg
Approval
ANDA ANDA076847
On the market since
Nov 17, 2009
Package NDCs
35356-439-09 35356-439-36
Official label
DailyMed (National Library of Medicine), updated Dec 11, 2024

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