Package 66758-071-38

Brand: ciloxan

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 66758-071-38
Digits Only 6675807138
Product NDC 66758-071
Description

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

Marketing

Marketing Status
Marketed Since 2025-03-28
Brand ciloxan
Generic ciprofloxacin hydrochloride
Sample Package No

Linked Drug Pages (1)

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"}