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Ciprofloxacin

Prescription ANDA TE AT Official labelling
Informational index, not medical advice. Content is reproduced from public FDA and NLM data. Always confirm against the manufacturer's current prescribing information. Report adverse events to FDA MedWatch.

Overview

Brand name
ciprofloxacin
Generic name
Ciprofloxacin
Dosage form
Solution
Route
Ophthalmic
Marketing category
ANDA · ANDA
Labeler
NuCare Pharmaceuticals,Inc.
Product type
Human Prescription Drug
DEA schedule
Not scheduled
Active ingredients
1
NDC product codes
11
Packages
17
Data completeness
83% of corroborating sources present

Active ingredients

Source: NDC Directory
Active ingredients and strengths as listed in the NDC Directory.
Ingredient Strength RxCUI Monograph
Ciprofloxacin Hydrochloride 3 mg/mL 309309 View

Forms, strengths and routes

Source: NDC Directory
Dosage form
Solution
Route of administration
Ophthalmic
Presentations
28

Pharmacologic classes are listed in the class section below.

Pharmacologic class

Source: NDC Directory
Established pharmacologic classes (EPC), mechanisms of action (MoA), chemical structures (CS) and physiologic effects (PE).
Class Type Browse
Cytochrome P450 1A2 Inhibitors [MoA] MoA All 31 members
Fluoroquinolone Antibacterial [EPC] EPC All 20 members
Fluoroquinolones [CS] CS All 20 members
Quinolone Antimicrobial [EPC] EPC All 16 members
Quinolones [CS] CS All 16 members

Regulatory status

Source: Drugs@FDANDC Directory
Application number
077568
Application type
ANDA · Abbreviated New Drug Application
Approval date
June 30, 2008
Sponsor
FDC LTD
Products on application
1
Submissions recorded
2
Products approved under application 077568.
Product Trade name Form Strength Ingredient Status TE Flags
077568-001 CIPROFLOXACIN HYDROCHLORIDE SOLUTION/DROPS CIPROFLOXACIN HYDROCHLORIDE Prescription AT

Therapeutic equivalence

Source: Orange Book
TE code
AT
Reference Listed Drug
No
Reference Standard
No

What this rating means: Therapeutically equivalent — bioequivalence demonstrated (topical dermatological products)

Codes beginning with “A” indicate products the FDA considers therapeutically equivalent. Codes beginning with “B” indicate bioequivalence has not been established. See methodology.

Approval history

Source: Drugs@FDA
Most recent submissions on application 077568.
Type No. Action Status Date Review
Supplement 6 Labeling Approved March 16, 2015 —
Original application 1 Approved June 30, 2008 —

Prescribing information

Source: openFDA Drug Labeling

Reproduced verbatim from the Structured Product Labeling submitted to the FDA (effective 20240612). This is the manufacturer's labelling text, not a summary and not advice.

HUMAN PRESCRIPTION DRUG · 20240612 HUMAN PRESCRIPTION DRUG · 20230902 HUMAN PRESCRIPTION DRUG · 20220502

Indications and Usage

openFDA Drug Labeling

INDICATIONS AND USAGE Ciprofloxacin ophthalmic solution is indicated for the treatment of infections caused by susceptible strains of the designated microorganisms in the conditions listed below: Corneal Ulcers: Pseudomonas aeruginosa Serratia marcescens * Staphylococcus aureus Staphylococcus epidermidis Streptococcus pneumoniae Streptococcus (Viridans Group) * Conjunctivitis: Haemophilus influenzae Staphylococcus aureus Staphylococcus epidermidis Streptococcus pneumoniae *Efficacy for this organism was studied in fewer than 10 infections.

Dosage and Administration

openFDA Drug Labeling

DOSAGE AND ADMINISTRATION Corneal Ulcers: The recommended dosage regimen for the treatment of corneal ulcers is two drops into the affected eye every 15 minutes for the first six hours and then two drops into the affected eye every 30 minutes for the remainder of the first day. On the second day, instill two drops in the affected eye hourly. On the third through the fourteenth day, place two drops in the affected eye every four hours. Treatment may be continued after 14 days if corneal re-epithelialisation has not occurred. Bacterial Conjunctivitis: The recommended dosage regimen for the treatment of bacterial conjunctivitis is one or two drops instilled into the conjunctival sac(s) every two hours while awake for two days and one or two drops every four hours while awake for the next five days.

Contraindications

openFDA Drug Labeling

CONTRAINDICATIONS A history of hypersensitivity to ciprofloxacin or any other component of the medication is a contraindication to its use. A history of hypersensitivity to other quinolones may also contraindicate the use of ciprofloxacin.

Warnings and Cautions

openFDA Drug Labeling

WARNINGS NOT FOR INJECTION INTO THE EYE. Serious and occasionally fatal hypersensitivity (anaphylactic) reactions, some following the first dose, have been reported in patients receiving systemic quinolone therapy. Some reactions were accompanied by cardiovascular collapse, loss of consciousness, tingling, pharyngeal or facial edema, dyspnea, urticaria, and itching. Only a few patients had a history of hypersensitivity reactions. Serious anaphylactic reactions require immediate emergency treatment with epinephrine and other resuscitation measures, including oxygen, intravenous fluids, intravenous antihistamines, corticosteroids, pressor amines and airway management, as clinically indicated. Remove contact lenses before using.

Adverse Reactions

openFDA Drug Labeling

ADVERSE REACTIONS The most frequently reported drug related adverse reaction was local burning or discomfort. In corneal ulcer studies with frequent administration of the drug, white crystalline precipitates were seen in approximately 17% of patients ( see Precautions ). Other reactions occurring in less than 10% of patients included lid margin crusting, crystals/scales, foreign body sensation, itching, conjunctival hyperemia and a bad taste following instillation. Additional events occurring in less than 1% of patients included corneal staining, keratopathy/keratitis, allergic reactions, lid edema, tearing, photophobia, corneal infiltrates, nausea and decreased vision. To report SUSPECTED ADVERSE REACTIONS, contact LEADING PHARMA AT 1-844-740-7500 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch

Drug Interactions

openFDA Drug Labeling

Drug Interactions: Specific drug interaction studies have not been conducted with ophthalmic ciprofloxacin. However, the systemic administration of some quinolones has been shown to elevate plasma concentrations of theophylline, interfere with the metabolism of caffeine, enhance the effects of the oral anticoagulant, warfarin, and its derivatives, and has been associated with transient elevations in serum creatinine in patients receiving cyclosporine concomitantly.

Description

openFDA Drug Labeling

DESCRIPTION Ciprofloxacin Ophthalmic Solution is a synthetic, sterile, multiple dose, antimicrobial for topical ophthalmic use. Ciprofloxacin is a fluoroquinolone antibacterial active against a broad spectrum of gram-positive and gram-negative ocular pathogens. It is available as the monohydrochloride monohydrate salt of 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinoline-carboxylic acid. It is a faint to light yellow crystalline powder with a molecular weight of 385.8. Its empirical formula is C 17 H 18 FN 3 O 3 •HCl•H 2 O and its chemical structure is as follows: Ciprofloxacin hydrochloride Ciprofloxacin differs from other quinolones in that it has a fluorine atom at the 6-position, a piperazine moiety at the 7-position, and a cyclopropyl ring at the 1-position. Each mL of Ciprofloxacin Ophthalmic Solution contains: Active: ciprofloxacin HCl 3.5 mg equivalent to 3 mg base. Preservative: benzalkonium chloride 0.006%. Inactives: sodium acetate, acetic acid, mannitol 4.6%, edetate disodium 0.05%, hydrochloric acid and/or sodium hydroxide (to adjust pH) and water for injection. The pH is approximately 4.5 and the osmolality is approximately 300 mOsm. Ciprofloxacin hydrochloride

OVERDOSAGE A topical overdose of Ciprofloxacin ophthalmic solution 0.3% may be flushed from the eye(s) with warm tap water.

How Supplied / Storage and Handling

openFDA Drug Labeling

HOW SUPPLIED As a sterile ophthalmic solution: 5 mL in translucent LDPE bottle with insert cap assembly comprising of a tan colored HDPE screw cap over a LDPE nozzle with tamper evident LDPE dust cover sealing the bottle cap. 5 mL – NDC 71205-300-05 STORAGE CONDITIONS Store at 25°C (77°F); excursions permitted 15°C to 30°C (59°F to 86°F) [See USP controlled room temperature]. Retain in carton until contents are used and protect from light. ANIMAL PHARMACOLOGY Ciprofloxacin and related drugs have been shown to cause arthropathy in immature animals of most species tested following oral administration. However, a one month topical ocular study using immature Beagle dogs did not demonstrate any articular lesions. CLINICAL STUDIES Following therapy with Ciprofloxacin ophthalmic solution, 76% of the patients with corneal ulcers and positive bacterial cultures were clinically cured and complete re-epithelialisation occurred in about 92% of the ulcers. In 3 and 7 day multicenter clinical trials, 52% of the patients with conjunctivitis and positive conjunctival cultures were clinically cured and 70-80% had all causative pathogens eradicated by the end of treatment. In a randomized, double-masked, multicenter, parallel-group clinical trial of pediatric patients with bacterial conjunctivitis, between birth and 31 days of age, patients were dosed with Ciprofloxacin ophthalmic solution or another anti-infective agent. Clinical outcomes for the trial demonstrated a clinical cure rate of 80% at Day 9 and a microbiological eradication success rate of 85% at Day 9. Please note that microbiologic eradication does not always correlate with clinical outcome in anti-infective trials. Rx Only Distributed by: Leading Pharma, LLC. Fairfield, NJ07004 Manufactured By: FDC Limited, B-8, MIDC Industrial Area, Waluj, Aurangabad - 431 136, Maharashtra, India Revision: 12/2017 STERILE OPHTHALMIC SOLUTION CIPROFLOXACIN OPHTHALMIC SOLUTION USP 0.3% as base INSTRUCTIONS FOR USE Read this Instruction for Use before you start using Ciprofloxacin ophthalmic solution and each time you get a refill. There may be new information. This information does not take the place of talking to your doctor about your medical condition or your treatment. Use Ciprofloxacin ophthalmic solution as prescribed by your doctor. Ask your doctor if you have questions about how to use Ciprofloxacin ophthalmic solution. Important information: • Ciprofloxacin ophthalmic solution is for use in the eye only. Ciprofloxacin ophthalmic solution should not be injected into the eye. • If you use other medicines in your eye, wait at least 10 minutes between using Ciprofloxacin ophthalmic solution and your other eye medicines. • If you wear contact lenses, remove them before using Ciprofloxacin ophthalmic solution. Wait at least 15 minutes after using Ciprofloxacin ophthalmic solution before placing your contact lenses back in your eyes. • Do not touch your eye, fingers, or other surfaces with the tip of the Ciprofloxacin ophthalmic solution bottle. You may get bacteria on the tip of the bottle that can cause you to get an eye infection. This eye infection can lead to serious eye damage or vision loss. If you think you have gotten bacteria on the tip of the bottle or you have an eye infection, call your doctor right away. • Wash your hands before each use. Before you use a bottle of Ciprofloxacin ophthalmic solution for the first time: • Check the expiration date on the bottle before use. Do not use Ciprofloxacin ophthalmic solution if the expiration date has passed. • Check that the seal on the dust cover is not broken or missing. Do not use the medicine if the seal is broken or missing. Call your doctor or pharmacist. Each time you use Ciprofloxacin ophthalmic solution: Step 1: Turn the dust cover clockwise to break the seal. Step 2: Remove the dust cover and throw it away. Step 3: Turn the tan coloured cap anti-clockwise and remove. Place the cap on a clean flat surface. Step 4: Tilt your head b …

Adverse event reports

Source: openFDA FAERS
96,908
FAERS reports mentioning this drug
as of 2026-09-25T03:42:24+00:00
A report count is not a risk measure. FAERS accepts voluntary and mandatory reports without establishing causation, and reporting is influenced by how widely a drug is used, how long it has been marketed, and media attention. FDA states that reports “do not prove that the drug caused the event”. Compare rates, not totals.

Attributed to this product's most-reported active ingredient: CIPROFLOXACIN HYDROCHLORIDE. Combination products with more than six active ingredients are not attributed, because a report count summed across a long ingredient list measures the list, not the medicine.

Recalls

Source: FDA Enforcement
Drug recall enforcement reports associated with this product.
Classification Reported Firm Reason Status
Class II March 26, 2025 FDC Limited Defective container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle Ongoing
Class II January 15, 2025 FDC Limited Defective container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle Ongoing
Class II August 7, 2024 FDC Limited Defective container: unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle. Ongoing

Packaging and NDCs

Source: NDC Directory
Every National Drug Code package associated with this medication. The NDC is the identifier used for dispensing, billing and pharmacovigilance in the United States.
Package NDC Product NDC Labeler Description Marketing start
50090-4217-0 50090-4217 A-S Medication Solutions 1 BOTTLE, PLASTIC in 1 CARTON (50090-4217-0) / 5 mL in 1 BOTTLE, PLASTIC March 26, 2019
80425-0499-1 80425-0499 Advanced Rx of Tennessee, LLC 1 BOTTLE, PLASTIC in 1 CARTON (80425-0499-1) / 5 mL in 1 BOTTLE, PLASTIC March 20, 2025
76420-588-02 76420-588 Asclemed USA, Inc. 1 BOTTLE, PLASTIC in 1 CARTON (76420-588-02) / 2.5 mL in 1 BOTTLE, PLASTIC September 2, 2023
76420-588-05 76420-588 Asclemed USA, Inc. 1 BOTTLE, PLASTIC in 1 CARTON (76420-588-05) / 5 mL in 1 BOTTLE, PLASTIC September 2, 2023
76420-588-10 76420-588 Asclemed USA, Inc. 1 BOTTLE, PLASTIC in 1 CARTON (76420-588-10) / 10 mL in 1 BOTTLE, PLASTIC September 2, 2023
85534-0075-0 85534-0075 HAWAII REPACK, INC 1 BOTTLE, PLASTIC in 1 CARTON (85534-0075-0) / 2.5 mL in 1 BOTTLE, PLASTIC July 12, 2026
85534-0075-1 85534-0075 HAWAII REPACK, INC 1 BOTTLE, PLASTIC in 1 CARTON (85534-0075-1) / 5 mL in 1 BOTTLE, PLASTIC July 12, 2026
85534-0075-2 85534-0075 HAWAII REPACK, INC 1 BOTTLE, PLASTIC in 1 CARTON (85534-0075-2) / 10 mL in 1 BOTTLE, PLASTIC July 12, 2026
69315-308-02 69315-308 Leading Pharma, LLC 1 BOTTLE, PLASTIC in 1 CARTON (69315-308-02) / 2.5 mL in 1 BOTTLE, PLASTIC November 1, 2018
69315-308-05 69315-308 Leading Pharma, LLC 1 BOTTLE, PLASTIC in 1 CARTON (69315-308-05) / 5 mL in 1 BOTTLE, PLASTIC November 1, 2018
69315-308-10 69315-308 Leading Pharma, LLC 1 BOTTLE, PLASTIC in 1 CARTON (69315-308-10) / 10 mL in 1 BOTTLE, PLASTIC November 1, 2018
68071-4672-3 68071-4672 NuCare Pharmaceuticals,Inc. 2.5 mL in 1 BOTTLE (68071-4672-3) December 18, 2018
68071-4679-5 68071-4679 NuCare Pharmaceuticals,Inc. 5 mL in 1 BOTTLE (68071-4679-5) December 26, 2018
68788-7500-5 68788-7500 Preferred Pharmaceuticals, Inc. 1 BOTTLE, PLASTIC in 1 CARTON (68788-7500-5) / 5 mL in 1 BOTTLE, PLASTIC November 30, 2019
71205-300-05 71205-300 Proficient Rx LP 1 BOTTLE, PLASTIC in 1 CARTON (71205-300-05) / 5 mL in 1 BOTTLE, PLASTIC November 1, 2018
67296-1703-9 67296-1703 Redpharm Drug 2 BOTTLE, PLASTIC in 1 CARTON (67296-1703-9) / 5 mL in 1 BOTTLE, PLASTIC November 1, 2018
85766-023-05 85766-023 Sportpharm LLC 1 BOTTLE, PLASTIC in 1 CARTON (85766-023-05) / 5 mL in 1 BOTTLE, PLASTIC August 5, 2025
50090-4217 50090-4217 A-S Medication Solutions — November 1, 2018
80425-0499 80425-0499 Advanced Rx of Tennessee, LLC — March 20, 2025
76420-588 76420-588 Asclemed USA, Inc. — November 1, 2018
85534-0075 85534-0075 HAWAII REPACK, INC — November 1, 2018
69315-308 69315-308 Leading Pharma, LLC — November 1, 2018
68071-4672 68071-4672 NuCare Pharmaceuticals,Inc. — November 1, 2018
68071-4679 68071-4679 NuCare Pharmaceuticals,Inc. — November 1, 2018
68788-7500 68788-7500 Preferred Pharmaceuticals, Inc. — November 1, 2018
71205-300 71205-300 Proficient Rx LP — November 1, 2018
67296-1703 67296-1703 Redpharm Drug — November 1, 2018
85766-023 85766-023 Sportpharm LLC — November 1, 2018

Sources for this page

Every dataset that contributed a fact to this page.
Dataset Agency Used for
NDC Directory FDA Identity, ingredients, strengths, forms, routes, labelers, packages
Drugs@FDA FDA Application, sponsor, submissions, review documents, marketing status
Orange Book FDA Therapeutic equivalence codes, reference drug flags, patents, exclusivity
Drug Labeling FDA / NLM Prescribing information reproduced above
FAERS FDA Adverse event report counts
Enforcement FDA Recall records

Generated September 25, 2026 · 13 sections on this page.