Ciprofloxacin 68071-2404
Product NDC
68071-2404- Manufacturer
- Nucare Pharmaceuticals,inc.
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 12, 2020
- Listing Expires
- December 31, 2027
- Application
- ANDA208921
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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, COATED in 1 BOTTLE (68071-2404-2)
4 TABLET, COATED in 1 BOTTLE (68071-2404-4)
6 TABLET, COATED in 1 BOTTLE (68071-2404-6)