Ciprofloxacin 72189-0616
Product NDC
72189-0616- Manufacturer
- Direct_rx
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 25, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA208921
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ciprofloxacin Hydrochloride | 250 mg/1 |
Drug Class
Cytochrome P450 1A2 Inhibitors [MoA]Fluoroquinolone Antibacterial [EPC]Fluoroquinolones [CS]
Packaging Options(1)
6 TABLET in 1 BOTTLE (72189-616-06)