NDC 85534-0069 – Ciprofloxacin

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

Human Prescription Drug

Product NDC85534-0069

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin Hydrochloride
Labeler
HAWAII REPACK, INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077859
Marketed since
April 26, 2007
Marketing end
January 31, 2027
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for ciprofloxacin →

Package NDC codes (7)

Package NDCDescriptionSince
85534-0069-06 TABLET, FILM COATED in 1 BOTTLE (85534-0069-0)Jul 13, 2026
85534-0069-110 TABLET, FILM COATED in 1 BOTTLE (85534-0069-1)Jul 13, 2026
85534-0069-214 TABLET, FILM COATED in 1 BOTTLE (85534-0069-2)Jul 13, 2026
85534-0069-320 TABLET, FILM COATED in 1 BOTTLE (85534-0069-3)Jul 13, 2026
85534-0069-421 TABLET, FILM COATED in 1 BOTTLE (85534-0069-4)Jul 13, 2026
85534-0069-528 TABLET, FILM COATED in 1 BOTTLE (85534-0069-5)Jul 13, 2026
85534-0069-630 TABLET, FILM COATED in 1 BOTTLE (85534-0069-6)Jul 13, 2026

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