Lofexidine hydrochloride
Active substance: lofexidine
TABLET, FILM COATED · LOFEXIDINE HYDROCHLORIDE .2 mg/1
United StatesActive
Marketing holder: Prasco Laboratories
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- LOFEXIDINE HYDROCHLORIDE · .2 mg/1
Import and control
Control by country
- United Statesprescription only
Source: openFDA NDC · record 01a1208d-aa27-7b17-bfe7-015530b5feb1,01a1208d-ed7b-7504-8803-d5fcdb5b9a0b,01a1208e-b32d-79b5-bc72-d12f621f3b7f,01a12097-bf54-7ad4-9b9a-df3401802dbc,01a1209c-3d47-745a-a99b-19fff846613f;count=8 · valid from 2026-10-09 · verified 2026-10-09
Registration
- Registration number
- 66993-345
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- ORAL
Sources
- product · openFDA NDC · 66993-345 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 66993-345 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 66993-345 · Verified 2026-10-09 · open in source