Ciprofloxacin Hydrochloride 72789-0577
Product NDC
72789-0577- Manufacturer
- Pd-Rx Pharmaceuticals, Inc.
- 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(3)
14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-577-14)
20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-577-20)
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-577-30)