Ciprofloxacin 61442-0224
Generic: Ciprofloxacin Hydrochloride
Product NDC
61442-0224- Manufacturer
- Carlsbad Technology, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 10, 2009
- Listing Expires
- December 31, 2026
- Application
- ANDA076126
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ciprofloxacin Hydrochloride | 750 mg/1 |
Drug Class
Cytochrome P450 1A2 Inhibitors [MoA]Fluoroquinolone Antibacterial [EPC]Fluoroquinolones [CS]
Packaging Options(2)
400 TABLET, FILM COATED in 1 BOTTLE (61442-224-04)
50 TABLET, FILM COATED in 1 BOTTLE (61442-224-50)