Nefazodone Hydrochloride
Active substance: nefazodone
TABLET · NEFAZODONE HYDROCHLORIDE 200 mg/1
United StatesActive
Marketing holder: Teva Pharmaceuticals USA, Inc.
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- NEFAZODONE HYDROCHLORIDE · 200 mg/1
Import and control
Control by country
- United Statesprescription only
Source: openFDA NDC · record 01a1208c-4a49-744a-8331-5cbd2ad45a13,01a1208c-fce6-7ddb-9369-c46c527249f8,01a1208d-010d-7cfb-a484-6c04b27f7da0,01a1208d-6ef6-761a-8d37-5602287d0fba,01a12091-7264-78a1-a89f-89c323739a1c;count=6 · valid from 2026-10-09 · verified 2026-10-09
Registration
- Registration number
- 0093-1025
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- ORAL
Sources
- product · openFDA NDC · 0093-1025 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 0093-1025 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 0093-1025 · Verified 2026-10-09 · open in source