Ciprofloxacin 70518-2837
Product NDC
70518-2837- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 18, 2020
- Listing Expires
- December 31, 2027
- Application
- ANDA076558
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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(1)
14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2837-4)