NDC 71205-649 – Ciprofloxacin

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

Human Prescription Drug

Product NDC71205-649

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin Hydrochloride
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077859
Marketed since
April 26, 2007
Listing expires
December 31, 2026
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for ciprofloxacin →

Package NDC codes (7)

Package NDCDescriptionSince
71205-649-066 TABLET, FILM COATED in 1 BOTTLE (71205-649-06)Mar 28, 2022
71205-649-077 TABLET, FILM COATED in 1 BOTTLE (71205-649-07)Jun 26, 2024
71205-649-1010 TABLET, FILM COATED in 1 BOTTLE (71205-649-10)Mar 28, 2022
71205-649-1414 TABLET, FILM COATED in 1 BOTTLE (71205-649-14)Mar 28, 2022
71205-649-2020 TABLET, FILM COATED in 1 BOTTLE (71205-649-20)Mar 28, 2022
71205-649-3030 TABLET, FILM COATED in 1 BOTTLE (71205-649-30)Mar 28, 2022
71205-649-6060 TABLET, FILM COATED in 1 BOTTLE (71205-649-60)Mar 28, 2022

Other ciprofloxacin products