Ciprofloxacin 66267-0716
Product NDC
66267-0716- Manufacturer
- Nucare Pharmaceuticals, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 10, 2004
- Listing Expires
- December 31, 2026
- Application
- ANDA076639
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ciprofloxacin Hydrochloride | 500 mg/1 |
Drug Class
Cytochrome P450 1A2 Inhibitors [MoA]Fluoroquinolone Antibacterial [EPC]Fluoroquinolones [CS]
Packaging Options(3)
2 TABLET in 1 BOTTLE (66267-716-02)
4 TABLET in 1 BOTTLE (66267-716-04)
6 TABLET in 1 BOTTLE (66267-716-06)