NDC 72162-1740 – Ciprofloxacin

Ciprofloxacin Hydrochloride 250 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC72162-1740

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076126
Marketed since
October 10, 2009
Listing expires
December 31, 2026
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for ciprofloxacin →

Package NDC codes (1)

Package NDCDescriptionSince
72162-1740-1100 TABLET, FILM COATED in 1 BOTTLE (72162-1740-1)Jul 16, 2024

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