NDC 0245-0211

Midodrine Hydrochloride 2.5 mg tablet

On the label: Upsher-Smith Laboratories, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Bora Pharmaceuticals Inc.Maple Grove, MN, United StatesMakes it and packages it Problems found, fixed voluntarilyAug 30, 2022 · 16 inspections

Product details

Generic drug
Midodrine: every company that makes it
Form
tablet, oral
Strength
2.5 mg
Approval
ANDA ANDA076725
On the market since
Nov 3, 2004
Package NDCs
0245-0211-01 0245-0211-11 0245-0211-89
Official label
DailyMed (National Library of Medicine), updated Jul 16, 2025

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