Carteolol Hydrochloride
Active substance: carteolol
SOLUTION · CARTEOLOL HYDROCHLORIDE 10 mg/mL
United StatesActive
Marketing holder: Sandoz Inc
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- CARTEOLOL HYDROCHLORIDE · 10 mg/mL
Import and control
Control by country
- United Statesprescription only
Source: openFDA NDC · record 01a12093-f06a-7a39-8a9a-1eb34040dead;count=1 · valid from 2026-10-09 · verified 2026-10-09
Registration
- Registration number
- 61314-238
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- OPHTHALMIC
Sources
- product · openFDA NDC · 61314-238 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 61314-238 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 61314-238 · Verified 2026-10-09 · open in source