Ciprofloxacin 72789-0125-50

Package NDC

72789-0125-50

Manufacturer: Pd-Rx Pharmaceuticals, Inc.
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: June 9, 2004
Listing Expires: December 31, 2026
Application: ANDA076558

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Active Ingredients

Ingredient	Strength
Ciprofloxacin Hydrochloride	750 mg/1

Drug Class

Cytochrome P450 1A2 Inhibitors [MoA]Fluoroquinolone Antibacterial [EPC]Fluoroquinolones [CS]

Selected Package

72789-0125-50Selected

50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-125-50)