Package 68071-4679-5

Brand: ciprofloxacin

Generic: ciprofloxacin
NDC Package

Package Facts

Identity

Package NDC 68071-4679-5
Digits Only 6807146795
Product NDC 68071-4679
Description

5 mL in 1 BOTTLE (68071-4679-5)

Marketing

Marketing Status
Marketed Since 2018-12-26
Brand ciprofloxacin
Generic ciprofloxacin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "1ab8822b-544e-2350-e063-6394a90ac9a9", "openfda": {"upc": ["0368071467956"], "unii": ["4BA73M5E37"], "rxcui": ["309307"], "spl_set_id": ["7def5a45-6725-0521-e053-2991aa0a0bda"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 BOTTLE (68071-4679-5)", "package_ndc": "68071-4679-5", "marketing_start_date": "20181226"}], "brand_name": "ciprofloxacin", "product_id": "68071-4679_1ab8822b-544e-2350-e063-6394a90ac9a9", "dosage_form": "SOLUTION", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "68071-4679", "generic_name": "Ciprofloxacin", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "3 mg/mL"}], "application_number": "ANDA077568", "marketing_category": "ANDA", "marketing_start_date": "20181101", "listing_expiration_date": "20261231"}