NDC 70518-3063 – Ciprofloxacin

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

Human Prescription Drug

Product NDC70518-3063

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076558
Marketed since
April 2, 2021
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
70518-3063-630 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3063-6)Aug 4, 2022

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