Ciprofloxacin 71335-2097
Product NDC
71335-2097- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 12, 2020
- Listing Expires
- December 31, 2027
- Application
- ANDA208921
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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(10)
7 TABLET, COATED in 1 BOTTLE (71335-2097-0)
20 TABLET, COATED in 1 BOTTLE (71335-2097-1)
10 TABLET, COATED in 1 BOTTLE (71335-2097-2)
14 TABLET, COATED in 1 BOTTLE (71335-2097-3)
6 TABLET, COATED in 1 BOTTLE (71335-2097-4)
30 TABLET, COATED in 1 BOTTLE (71335-2097-5)
60 TABLET, COATED in 1 BOTTLE (71335-2097-6)
12 TABLET, COATED in 1 BOTTLE (71335-2097-7)
40 TABLET, COATED in 1 BOTTLE (71335-2097-8)
90 TABLET, COATED in 1 BOTTLE (71335-2097-9)