Package 68071-4139-5
Brand: ciprofloxacin hydrochloride
Generic: ciprofloxacin hydrochloridePackage Facts
Identity
Package NDC
68071-4139-5
Digits Only
6807141395
Product NDC
68071-4139
Description
5 mL in 1 BOX (68071-4139-5)
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": "2d3feef9-74ea-c651-e063-6394a90a2ca3", "openfda": {"upc": ["0368071413953"], "unii": ["4BA73M5E37"], "rxcui": ["309307"], "spl_set_id": ["5cf0f572-48fc-6a3a-e053-2991aa0a8437"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 BOX (68071-4139-5)", "package_ndc": "68071-4139-5", "marketing_start_date": "20171101"}], "brand_name": "Ciprofloxacin Hydrochloride", "product_id": "68071-4139_2d3feef9-74ea-c651-e063-6394a90a2ca3", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "68071-4139", "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"}