benzphetamine hydrochloride
Active substance: benzphetamine
TABLET · BENZPHETAMINE HYDROCHLORIDE 50 mg/1
United StatesActive
Marketing holder: Calvin Scott & Co., Inc.
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- BENZPHETAMINE HYDROCHLORIDE · 50 mg/1
Import and control
Control by country
- United StatescontrolledSchedule: CIII
Source: openFDA NDC · record 01a1208c-c236-7368-b6eb-ffea233f02e3,01a1208d-17c6-74cb-8c8c-4cc271292500,01a12098-6d2d-73cb-b5da-6352c514a641,01a1209a-bd55-719e-9da1-910e3dd4dacd,01a1209a-c7c8-7ab1-85be-247114660c1d;count=6 · valid from 2026-10-09 · verified 2026-10-09
Registration
- Registration number
- 17224-672
- Registration status
- Active
- Dispensing
- Prescription only
- Control marker
- CIII
- Route
- ORAL
Sources
- product · openFDA NDC · 17224-672 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 17224-672 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 17224-672 · Verified 2026-10-09 · open in source