Midodrine Hydrochloride
Active substance: midodrine
TABLET · MIDODRINE HYDROCHLORIDE 5 mg/1
United StatesActive
Marketing holder: AvPAK
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- MIDODRINE HYDROCHLORIDE · 5 mg/1
Import and control
Control by country
- United Statesprescription only
Source: openFDA NDC · record 01a1208c-294c-7ca7-85a4-c02ebdba093f,01a1208c-299d-7a3a-9771-8ffd7818c677,01a1208c-2d30-796d-9b5b-ca1d5bbf7f77,01a1208c-2d73-7478-9d83-9148c09357ca,01a1208c-3fd1-76ca-8eb4-73252438dfc5;count=109 · valid from 2026-10-09 · verified 2026-10-09
Registration
- Registration number
- 50268-562
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- ORAL
Sources
- product · openFDA NDC · 50268-562 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 50268-562 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 50268-562 · Verified 2026-10-09 · open in source