DESIPRAMINE HYDROCHLORIDE
Active substance: desipramine
TABLET, FILM COATED · DESIPRAMINE HYDROCHLORIDE 50 mg/1
United StatesActive
Marketing holder: Alembic Pharmaceuticals Limited
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- DESIPRAMINE HYDROCHLORIDE · 50 mg/1
Import and control
Control by country
- United Statesprescription only
Source: openFDA NDC · record 01a1208c-4fb4-756c-b747-f10196cb4c99,01a1208c-61e1-74f9-8ce8-5c87dbb10ff3,01a1208c-624b-724b-bb4f-b03a7d6daf98,01a1208c-624c-7c53-bba1-fbc4fafd0084,01a1208c-8847-7797-8599-596d8afd1223;count=45 · valid from 2026-10-09 · verified 2026-10-09
Registration
- Registration number
- 46708-317
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- ORAL
Sources
- product · openFDA NDC · 46708-317 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 46708-317 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 46708-317 · Verified 2026-10-09 · open in source