NDC 83708-111

Bondlido 200 mg system

On the label: MEDRx USA, Inc..

Taiwan: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Delta Synthetic Co., Ltd.Tucheng District, TaiwanMakes the active ingredient and tests it No problems foundMay 29, 2025 · 6 inspections
Sumika Chemical Analysis Service, Ltd.Oita, JapanTests it No problems foundNov 7, 2025 · 6 inspections

Product details

Generic drug
Lidocaine: every company that makes it
Form
system, topical
Strength
200 mg
Approval
NDA NDA215029
On the market since
Oct 8, 2025
Package NDCs
83708-111-01 83708-111-28
Official label
DailyMed (National Library of Medicine), updated Oct 6, 2025

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