NDC 71335-1229 – Ciprofloxacin

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

Human Prescription Drug

Product NDC71335-1229

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin Tablets
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA208921
Marketed since
July 13, 2019
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
71335-1229-07 TABLET, COATED in 1 BOTTLE (71335-1229-0)Jan 30, 2025
71335-1229-114 TABLET, COATED in 1 BOTTLE (71335-1229-1)Jan 30, 2025
71335-1229-230 TABLET, COATED in 1 BOTTLE (71335-1229-2)Sep 9, 2019
71335-1229-320 TABLET, COATED in 1 BOTTLE (71335-1229-3)Jan 30, 2025
71335-1229-460 TABLET, COATED in 1 BOTTLE (71335-1229-4)Jan 30, 2025
71335-1229-56 TABLET, COATED in 1 BOTTLE (71335-1229-5)Jul 19, 2019
71335-1229-610 TABLET, COATED in 1 BOTTLE (71335-1229-6)Jan 30, 2025
71335-1229-728 TABLET, COATED in 1 BOTTLE (71335-1229-7)Jan 30, 2025
71335-1229-8100 TABLET, COATED in 1 BOTTLE (71335-1229-8)Jan 30, 2025
71335-1229-940 TABLET, COATED in 1 BOTTLE (71335-1229-9)Jan 30, 2025

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