Ciprofloxacin 42708-0192

Product NDC

42708-0192

Manufacturer: Qpharma, Inc.
Dosage Form: Tablet, Film Coated
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(1)

42708-0192-14

14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-192-14)

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