Ciprofloxacin
Active substance: ciprofloxacin
TABLET, FILM COATED · CIPROFLOXACIN HYDROCHLORIDE 500 mg/1
United StatesActive
Marketing holder: PD-Rx Pharmaceuticals, Inc.
Verified 2026-10-09 · openFDA NDC
Analogues in other countries- Source: openFDA NDC
- Countries with the substance registered: 2
Composition
- CIPROFLOXACIN HYDROCHLORIDE · 500 mg/1
Analogues by country
Products with the same active substance registered in other countries.
| Country | Products |
|---|---|
| RU 150 |
|
Import and control
Control by country
- United Statesprescription only
Source: openFDA NDC · record 01a1208c-2d04-7730-9353-34bcd906003e,01a1208c-325a-775a-b827-ec4ed45758a2,01a1208c-34ac-7ba4-8ab7-c1dbbd2edd58,01a1208c-4a77-71b7-9037-1423fd97725c,01a1208c-4a78-773d-a5ac-e7fec5ad3840;count=206 · valid from 2026-10-09 · verified 2026-10-09
Registration
- Registration number
- 72789-520
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- ORAL
Sources
- product · openFDA NDC · 72789-520 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 72789-520 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 72789-520 · Verified 2026-10-09 · open in source