Ciprofloxacin 72789-0193
Product NDC
72789-0193- Manufacturer
- Pd-Rx Pharmaceuticals, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 9, 2004
- Listing Expires
- December 31, 2026
- 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(5)
6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-193-06)
10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-193-10)
12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-193-12)
14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-193-14)
20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-193-20)