NDC 71335-2054 – Ciprofloxacin

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

Human Prescription Drug

Product NDC71335-2054

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA208921
Marketed since
August 12, 2020
Listing expires
December 31, 2027
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for ciprofloxacin →

Package NDC codes (10)

Package NDCDescriptionSince
71335-2054-07 TABLET, COATED in 1 BOTTLE (71335-2054-0)Apr 3, 2024
71335-2054-114 TABLET, COATED in 1 BOTTLE (71335-2054-1)Mar 20, 2023
71335-2054-230 TABLET, COATED in 1 BOTTLE (71335-2054-2)Mar 21, 2022
71335-2054-320 TABLET, COATED in 1 BOTTLE (71335-2054-3)Mar 17, 2023
71335-2054-460 TABLET, COATED in 1 BOTTLE (71335-2054-4)Jun 1, 2023
71335-2054-56 TABLET, COATED in 1 BOTTLE (71335-2054-5)Aug 31, 2023
71335-2054-610 TABLET, COATED in 1 BOTTLE (71335-2054-6)Jun 21, 2023
71335-2054-728 TABLET, COATED in 1 BOTTLE (71335-2054-7)Mar 28, 2023
71335-2054-8100 TABLET, COATED in 1 BOTTLE (71335-2054-8)Apr 3, 2024
71335-2054-940 TABLET, COATED in 1 BOTTLE (71335-2054-9)Apr 3, 2024

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