NDC 70518-4214 – Ciprofloxacin

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

Human Prescription Drug

Product NDC70518-4214

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077859
Marketed since
October 15, 2024
Marketing end
February 29, 2028
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Ciprofloxacin →

Package NDC codes (4)

Package NDCDescriptionSince
70518-4214-030 TABLET, FILM COATED in 1 BLISTER PACK (70518-4214-0)Oct 15, 2024
70518-4214-114 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4214-1)Oct 25, 2024
70518-4214-214 TABLET, FILM COATED in 1 BLISTER PACK (70518-4214-2)Nov 13, 2024
70518-4214-310 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4214-3)May 12, 2026

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