NDC 55154-0193 – ciprofloxacin

Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC55154-0193

Product details

Brand name
ciprofloxacin
Generic name
ciprofloxacin
Labeler
Cardinal Health 107, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076639
Marketed since
October 17, 2025
Listing expires
December 31, 2027
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for ciprofloxacin →

Package NDC codes (1)

Package NDCDescriptionSince
55154-0193-010 BLISTER PACK in 1 BAG (55154-0193-0) / 1 TABLET, FILM COATED in 1 BLISTER PACKOct 17, 2025

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