Ciprofloxacin 71205-0649
Generic: Ciprofloxacin Hydrochloride
Product NDC
71205-0649- Manufacturer
- Proficient Rx Lp
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 26, 2007
- Listing Expires
- December 31, 2026
- Application
- ANDA077859
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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(7)
6 TABLET, FILM COATED in 1 BOTTLE (71205-649-06)
7 TABLET, FILM COATED in 1 BOTTLE (71205-649-07)
10 TABLET, FILM COATED in 1 BOTTLE (71205-649-10)
14 TABLET, FILM COATED in 1 BOTTLE (71205-649-14)
20 TABLET, FILM COATED in 1 BOTTLE (71205-649-20)
30 TABLET, FILM COATED in 1 BOTTLE (71205-649-30)
60 TABLET, FILM COATED in 1 BOTTLE (71205-649-60)