Ciprofloxacin 43063-0869
Product NDC
43063-0869- 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 | 500 mg/1 |
Drug Class
Cytochrome P450 1A2 Inhibitors [MoA]Fluoroquinolone Antibacterial [EPC]Fluoroquinolones [CS]
Packaging Options(5)
6 TABLET in 1 BOTTLE, PLASTIC (43063-869-06)
8 TABLET in 1 BOTTLE, PLASTIC (43063-869-08)
10 TABLET in 1 BOTTLE, PLASTIC (43063-869-10)
20 TABLET in 1 BOTTLE, PLASTIC (43063-869-20)
30 TABLET in 1 BOTTLE, PLASTIC (43063-869-30)