NDC 82868-070 – Ciprofloxacin

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

Human Prescription Drug

Product NDC82868-070

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin Hydrochloride
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077859
Marketed since
January 21, 2025
Marketing end
January 31, 2027
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for ciprofloxacin →

Package NDC codes (2)

Package NDCDescriptionSince
82868-070-1414 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-070-14)Feb 10, 2025
82868-070-2020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-070-20)Jan 21, 2025

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