LABETALOL HYDROCHLORIDE
Active substance: labetalol
TABLET, FILM COATED · LABETALOL HYDROCHLORIDE 200 mg/1
United StatesActive
Marketing holder: A-S Medication Solutions
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- LABETALOL HYDROCHLORIDE · 200 mg/1
Import and control
Control by country
- United Statesprescription only
Source: openFDA NDC · record 01a1208c-2d74-78ae-86bf-792bea57d25e,01a1208c-4cf4-7b37-87e3-daa1e6160edf,01a1208c-51ab-76c9-8943-471c886b09df,01a1208c-56fe-7f8e-aab9-913fc61e02d8,01a1208c-58c1-7b96-9345-90c258d7d690;count=142 · valid from 2026-10-09 · verified 2026-10-09
Registration
- Registration number
- 50090-6774
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- ORAL
Sources
- product · openFDA NDC · 50090-6774 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 50090-6774 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 50090-6774 · Verified 2026-10-09 · open in source