NDC 71335-2046 – Ciprofloxacin

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

Human Prescription Drug

Product NDC71335-2046

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin Hydrochloride
Labeler
Bryant Ranch Prepack
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 (10)

Package NDCDescriptionSince
71335-2046-07 TABLET, FILM COATED in 1 BOTTLE (71335-2046-0)Apr 3, 2024
71335-2046-114 TABLET, FILM COATED in 1 BOTTLE (71335-2046-1)Feb 16, 2022
71335-2046-230 TABLET, FILM COATED in 1 BOTTLE (71335-2046-2)Mar 1, 2022
71335-2046-320 TABLET, FILM COATED in 1 BOTTLE (71335-2046-3)Feb 16, 2022
71335-2046-460 TABLET, FILM COATED in 1 BOTTLE (71335-2046-4)Jun 20, 2022
71335-2046-56 TABLET, FILM COATED in 1 BOTTLE (71335-2046-5)May 17, 2022
71335-2046-610 TABLET, FILM COATED in 1 BOTTLE (71335-2046-6)Feb 15, 2022
71335-2046-728 TABLET, FILM COATED in 1 BOTTLE (71335-2046-7)Mar 7, 2022
71335-2046-8100 TABLET, FILM COATED in 1 BOTTLE (71335-2046-8)Nov 29, 2022
71335-2046-940 TABLET, FILM COATED in 1 BOTTLE (71335-2046-9)Apr 3, 2024

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