Protriptyline Hydrochloride
Active substance: protriptyline
TABLET, FILM COATED · PROTRIPTYLINE HYDROCHLORIDE 10 mg/1
United StatesActive
Marketing holder: Sigmapharm Laboratories, LLC
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- PROTRIPTYLINE HYDROCHLORIDE · 10 mg/1
Import and control
Control by country
- United Statesprescription only
Source: openFDA NDC · record 01a1208d-1798-73b8-9810-e14cacb1b568,01a1208f-aa07-741a-8166-9fbb71767505,01a1208f-aa0c-7bad-bb78-ade8846e0b5f,01a12093-69c4-71e2-8bbe-a782f67130d4;count=4 · valid from 2026-10-09 · verified 2026-10-09
Registration
- Registration number
- 42794-007
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- ORAL
Sources
- product · openFDA NDC · 42794-007 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 42794-007 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 42794-007 · Verified 2026-10-09 · open in source