Package 68071-4139-5

Brand: ciprofloxacin hydrochloride

Generic: ciprofloxacin hydrochloride
NDC Package

Package 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
Marketed Since 2017-11-01
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"}