AMPICILLIN
Active substance: ampicillin
POWDER, FOR SOLUTION · AMPICILLIN SODIUM 250 mg/250mg
United StatesActive
Marketing holder: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Verified 2026-10-09 · openFDA NDC
Analogues in other countries- Source: openFDA NDC
- Countries with the substance registered: 2
Composition
- AMPICILLIN SODIUM · 250 mg/250mg
Analogues by country
Products with the same active substance registered in other countries.
| Country | Products |
|---|---|
| RU 107 |
|
Import and control
Control by country
- United Statesprescription only
Source: openFDA NDC · record 01a1208c-3b45-7eee-b8b2-461ffaf437c5,01a1208c-3b46-7f71-88b4-126edf5f5683,01a1208c-3fa9-715f-8934-c46a0dce0ebe,01a1208c-3fab-7c4f-b895-21cfc08ff18c,01a1208c-4d14-7cae-961c-feb4c8bd08fe;count=74 · valid from 2026-10-09 · verified 2026-10-09
Registration
- Registration number
- 23155-914
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- INTRAMUSCULAR, INTRAVENOUS
Sources
- product · openFDA NDC · 23155-914 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 23155-914 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 23155-914 · Verified 2026-10-09 · open in source