NDC 71205-905

Midodrine Hydrochloride 5 mg tablet

On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Xiromed, LLC.'s NDC 70700-158.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Cerovene, Inc.Valley Cottage, NY, United StatesMakes it and tests it Problems found, fixed voluntarilyMar 23, 2026 · 9 inspections
Nutra-Med Packaging LLCWhippany, NJ, United StatesPackages it No problems foundNov 20, 2024 · 6 inspections

Repackaging site

Product details

Generic drug
Midodrine: every company that makes it
Form
tablet, oral
Strength
5 mg
Approval
ANDA ANDA207849
On the market since
Oct 15, 2020
Package NDCs
71205-905-00 71205-905-11 71205-905-30 71205-905-55 71205-905-60 71205-905-72 71205-905-90
Official label
DailyMed (National Library of Medicine), updated Apr 1, 2022

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