Ciprofloxacin 68788-8200
Product NDC
68788-8200- Manufacturer
- Preferred Pharmaceuticals Inc.
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 24, 2022
- Listing Expires
- December 31, 2027
- 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(3)
10 TABLET, COATED in 1 BOTTLE (68788-8200-1)
20 TABLET, COATED in 1 BOTTLE (68788-8200-2)
30 TABLET, COATED in 1 BOTTLE (68788-8200-3)