Ciprofloxacin 68071-3699
Generic: Ciprofolxacin
Product NDC
68071-3699- Manufacturer
- Nucare Pharmaceutical, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 1, 2023
- 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(4)
10 TABLET in 1 BOTTLE (68071-3699-1)
20 TABLET in 1 BOTTLE (68071-3699-2)
30 TABLET in 1 BOTTLE (68071-3699-3)
6 TABLET in 1 BOTTLE (68071-3699-6)