Package 68071-4235-3
Brand: ciprofloxacin hydrochloride
Generic: ciprofloxacin hydrochloridePackage Facts
Identity
Package NDC
68071-4235-3
Digits Only
6807142353
Product NDC
68071-4235
Description
2.5 mL in 1 BOX (68071-4235-3)
Marketing
Marketing Status
Brand
ciprofloxacin hydrochloride
Generic
ciprofloxacin hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "2d3ff27f-de04-c79c-e063-6294a90a05c3", "openfda": {"upc": ["0368071423532"], "unii": ["4BA73M5E37"], "rxcui": ["309307"], "spl_set_id": ["6301febb-01aa-1af5-e053-2991aa0aa309"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "2.5 mL in 1 BOX (68071-4235-3)", "package_ndc": "68071-4235-3", "marketing_start_date": "20180117"}], "brand_name": "Ciprofloxacin Hydrochloride", "product_id": "68071-4235_2d3ff27f-de04-c79c-e063-6294a90a05c3", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "68071-4235", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin Hydrochloride", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "3 mg/mL"}], "application_number": "NDA019992", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20040507", "listing_expiration_date": "20261231"}