PANTOPRAZOLE SODIUM
Active substance: pantoprazole
TABLET, DELAYED RELEASE · PANTOPRAZOLE SODIUM 40 mg/1
United StatesActive
Marketing holder: Asclemed USA, Inc.
Verified 2026-10-09 · openFDA NDC
Analogues in other countries- Source: openFDA NDC
- Countries with the substance registered: 3
Composition
- PANTOPRAZOLE SODIUM · 40 mg/1
Analogues by country
Products with the same active substance registered in other countries.
| Country | Products |
|---|---|
| RU 52 |
|
| EU 5 |
|
Import and control
Control by country
- United Statesprescription only
Source: openFDA NDC · record 01a1208c-273f-79a6-8b73-2b0f84a367db,01a1208c-2cbb-7820-aee7-d082ac318867,01a1208c-2d60-7325-89cd-2512d48c487e,01a1208c-323f-7b72-b727-fa87895e2df6,01a1208c-404a-710e-b81c-4621e3789992;count=166 · valid from 2026-10-09 · verified 2026-10-09
Registration
- Registration number
- 76420-674
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- ORAL
Sources
- product · openFDA NDC · 76420-674 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 76420-674 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 76420-674 · Verified 2026-10-09 · open in source