Ciprofloxacin 71335-0070
Product NDC
71335-0070- Manufacturer
- Bryant Ranch Prepack
- 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(10)
7 TABLET in 1 BOTTLE (71335-0070-0)
14 TABLET in 1 BOTTLE (71335-0070-1)
30 TABLET in 1 BOTTLE (71335-0070-2)
20 TABLET in 1 BOTTLE (71335-0070-3)
60 TABLET in 1 BOTTLE (71335-0070-4)
6 TABLET in 1 BOTTLE (71335-0070-5)
10 TABLET in 1 BOTTLE (71335-0070-6)
28 TABLET in 1 BOTTLE (71335-0070-7)
100 TABLET in 1 BOTTLE (71335-0070-8)
40 TABLET in 1 BOTTLE (71335-0070-9)