NDC 82868-102 – Ciprofloxacin

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

Human Prescription Drug

Product NDC82868-102

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076639
Marketed since
February 12, 2026
Listing expires
December 31, 2027
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Ciprofloxacin →

Package NDC codes (2)

Package NDCDescriptionSince
82868-102-1414 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-102-14)Feb 12, 2026
82868-102-2020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-102-20)Jul 21, 2026

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