Ciprofloxacin Hydrochloride 67296-2208
Product NDC
67296-2208- Manufacturer
- Redpharm Drug
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 23, 2024
- Listing Expires
- December 31, 2027
- Application
- ANDA076593
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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 (67296-2208-1)