Ciprofloxacin 42708-0088
Product NDC
42708-0088- Manufacturer
- Qpharma Inc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 26, 2007
- Application
- ANDA077859
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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)
14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-088-14)