Ciprofloxacin 68071-2267
Product NDC
68071-2267- Manufacturer
- Nucare Pharmaceuticals,inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 1, 2006
- Listing Expires
- December 31, 2026
- Application
- ANDA076794
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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(1)
10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-2267-1)