NDC 72189-627 – Ciprofloxacin

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

Human Prescription Drug

Product NDC72189-627

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
Direct_Rx
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077859
Marketed since
June 5, 2025
Marketing end
February 29, 2028
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Ciprofloxacin →

Package NDC codes (2)

Package NDCDescriptionSince
72189-627-1010 TABLET, FILM COATED in 1 BOTTLE (72189-627-10)Jun 5, 2025
72189-627-1414 TABLET, FILM COATED in 1 BOTTLE (72189-627-14)Jun 5, 2025

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