ciloxan

Generic: ciprofloxacin hydrochloride

Labeler: sandoz inc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name ciloxan
Generic Name ciprofloxacin hydrochloride
Labeler sandoz inc
Dosage Form OINTMENT
Routes
OPHTHALMIC
Active Ingredients

ciprofloxacin hydrochloride 3 mg/g

Manufacturer
Sandoz Inc

Identifiers & Regulatory

Product NDC 66758-071
Product ID 66758-071_930a2e4b-dcac-4a27-a073-fd21622c1666
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA020369
Listing Expiration 2026-12-31
Marketing Start 1998-06-02

Pharmacologic Class

Classes
cytochrome p450 1a2 inhibitors [moa] fluoroquinolone antibacterial [epc] fluoroquinolones [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 66758071
Hyphenated Format 66758-071

Supplemental Identifiers

RxCUI
213307 309306
UPC
0366758071380
UNII
4BA73M5E37

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name ciloxan (source: ndc)
Generic Name ciprofloxacin hydrochloride (source: ndc)
Application Number NDA020369 (source: ndc)
Routes
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • 3 mg/g
source: ndc
Packaging
  • 3.5 g in 1 TUBE (66758-071-38)
source: ndc

Packages (1)

66758-071-38 3.5 g in 1 TUBE (66758-071-38)

Ingredients (1)

ciprofloxacin hydrochloride (3 mg/g)

Linked Drug Pages (1)

CILOXAN ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "930a2e4b-dcac-4a27-a073-fd21622c1666", "openfda": {"upc": ["0366758071380"], "unii": ["4BA73M5E37"], "rxcui": ["213307", "309306"], "spl_set_id": ["09ca5374-2a16-4a95-91b3-70591d78254e"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3.5 g in 1 TUBE (66758-071-38)", "package_ndc": "66758-071-38", "marketing_start_date": "20250328"}], "brand_name": "CILOXAN", "product_id": "66758-071_930a2e4b-dcac-4a27-a073-fd21622c1666", "dosage_form": "OINTMENT", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "66758-071", "generic_name": "ciprofloxacin hydrochloride", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CILOXAN", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "3 mg/g"}], "application_number": "NDA020369", "marketing_category": "NDA", "marketing_start_date": "19980602", "listing_expiration_date": "20261231"}