NDC 70518-2837 – Ciprofloxacin

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

Human Prescription Drug

Product NDC70518-2837

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076558
Marketed since
August 18, 2020
Listing expires
December 31, 2027
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Ciprofloxacin →

Package NDC codes (1)

Package NDCDescriptionSince
70518-2837-414 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2837-4)Feb 5, 2023

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