Ciprofloxacin Hydrochloride 69367-0385-01

Package NDC

69367-0385-01

Manufacturer: Westminster Pharmaceuticals, Llc
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: May 23, 2024
Listing Expires: December 31, 2026
Application: ANDA076593

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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]

Selected Package

69367-0385-01Selected

100 TABLET, FILM COATED in 1 BOTTLE (69367-385-01)