Package 68071-4122-4

Brand: ciprofloxacin

Generic: ciprofloxacin
NDC Package

Package Facts

Identity

Package NDC 68071-4122-4
Digits Only 6807141224
Product NDC 68071-4122
Description

14 TABLET in 1 BOTTLE (68071-4122-4)

Marketing

Marketing Status
Marketed Since 2017-10-16
Brand ciprofloxacin
Generic ciprofloxacin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1a13ecfc-3490-4377-e063-6394a90ad455", "openfda": {"upc": ["0368071412222"], "unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["5bab9397-b9f3-d309-e053-2991aa0a6612"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (68071-4122-1)", "package_ndc": "68071-4122-1", "marketing_start_date": "20171016"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (68071-4122-2)", "package_ndc": "68071-4122-2", "marketing_start_date": "20171016"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-4122-3)", "package_ndc": "68071-4122-3", "marketing_start_date": "20171016"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (68071-4122-4)", "package_ndc": "68071-4122-4", "marketing_start_date": "20171016"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-4122-6)", "package_ndc": "68071-4122-6", "marketing_start_date": "20171016"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE (68071-4122-7)", "package_ndc": "68071-4122-7", "marketing_start_date": "20171016"}], "brand_name": "ciprofloxacin", "product_id": "68071-4122_1a13ecfc-3490-4377-e063-6394a90ad455", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "68071-4122", "generic_name": "ciprofloxacin", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA076639", "marketing_category": "ANDA", "marketing_start_date": "20040910", "listing_expiration_date": "20261231"}