Ciprofloxacin 68071-2267-01

Package NDC

68071-2267-01

Manufacturer: Nucare Pharmaceuticals,inc.
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: November 1, 2006
Listing Expires: December 31, 2026
Application: ANDA076794

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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]

Selected Package

68071-2267-01Selected

10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-2267-1)