Ciprofloxacin 43063-0767
Product NDC
43063-0767- Manufacturer
- Pd-Rx Pharmaceuticals, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 10, 2004
- Listing Expires
- December 31, 2026
- Application
- ANDA076639
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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(1)
28 TABLET in 1 BOTTLE, PLASTIC (43063-767-28)