Package 68071-4576-6

Brand: ciprofloxacin

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-4576-6
Digits Only 6807145766
Product NDC 68071-4576
Description

60 TABLET, FILM COATED in 1 BOTTLE (68071-4576-6)

Marketing

Marketing Status
Marketed Since 2018-09-27
Brand ciprofloxacin
Generic ciprofloxacin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1ab541b5-e90a-a1f7-e063-6294a90a0f25", "openfda": {"upc": ["0368071457629"], "unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["76dedf59-46be-1be0-e053-2991aa0a1c36"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET, FILM COATED in 1 BOTTLE (68071-4576-1)", "package_ndc": "68071-4576-1", "marketing_start_date": "20180927"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68071-4576-2)", "package_ndc": "68071-4576-2", "marketing_start_date": "20180927"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-4576-3)", "package_ndc": "68071-4576-3", "marketing_start_date": "20180927"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (68071-4576-4)", "package_ndc": "68071-4576-4", "marketing_start_date": "20180927"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68071-4576-6)", "package_ndc": "68071-4576-6", "marketing_start_date": "20180927"}], "brand_name": "Ciprofloxacin", "product_id": "68071-4576_1ab541b5-e90a-a1f7-e063-6294a90a0f25", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "68071-4576", "generic_name": "Ciprofloxacin Hydrochloride", "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": "ANDA077859", "marketing_category": "ANDA", "marketing_start_date": "20070426", "listing_expiration_date": "20261231"}