NDC 82804-130 – Ciprofloxacin

Ciprofloxacin Hydrochloride 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC82804-130

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofolxacin
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208921
Marketed since
October 1, 2023
Listing expires
December 31, 2026
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for ciprofloxacin →

Package NDC codes (5)

Package NDCDescriptionSince
82804-130-066 TABLET in 1 BOTTLE (82804-130-06)Sep 5, 2024
82804-130-1010 TABLET in 1 BOTTLE (82804-130-10)Sep 5, 2024
82804-130-1414 TABLET in 1 BOTTLE (82804-130-14)Sep 5, 2024
82804-130-2020 TABLET in 1 BOTTLE (82804-130-20)Sep 5, 2024
82804-130-3030 TABLET in 1 BOTTLE (82804-130-30)Apr 28, 2025

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