NDC 71335-1867 – Ciprofloxacin

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

Human Prescription Drug

Product NDC71335-1867

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076558
Marketed since
June 9, 2004
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
71335-1867-07 TABLET, FILM COATED in 1 BOTTLE (71335-1867-0)Feb 14, 2022
71335-1867-120 TABLET, FILM COATED in 1 BOTTLE (71335-1867-1)May 10, 2021
71335-1867-210 TABLET, FILM COATED in 1 BOTTLE (71335-1867-2)Aug 4, 2021
71335-1867-314 TABLET, FILM COATED in 1 BOTTLE (71335-1867-3)Jul 12, 2021
71335-1867-46 TABLET, FILM COATED in 1 BOTTLE (71335-1867-4)Oct 11, 2021
71335-1867-530 TABLET, FILM COATED in 1 BOTTLE (71335-1867-5)Feb 14, 2022
71335-1867-660 TABLET, FILM COATED in 1 BOTTLE (71335-1867-6)Feb 14, 2022
71335-1867-712 TABLET, FILM COATED in 1 BOTTLE (71335-1867-7)Feb 14, 2022
71335-1867-840 TABLET, FILM COATED in 1 BOTTLE (71335-1867-8)Feb 14, 2022
71335-1867-990 TABLET, FILM COATED in 1 BOTTLE (71335-1867-9)Feb 14, 2022

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