Package 68071-2267-1

Brand: ciprofloxacin

Generic: ciprofloxacin
NDC Package

Package Facts

Identity

Package NDC 68071-2267-1
Digits Only 6807122671
Product NDC 68071-2267
Product ID 68071-2267_1d76786e-4b8e-9489-e063-6294a90a2a17
Description

10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-2267-1)

Marketing

Marketing Status
Marketed Since 2020-09-24
Brand ciprofloxacin
Generic ciprofloxacin
Sample Package No

Linked Drug Pages (1)

Ciprofloxacin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1d76786e-4b8e-9489-e063-6294a90a2a17", "openfda": {"upc": ["0368071226713"], "unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["b0136d72-0869-2da0-e053-2995a90af70a"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-2267-1)", "package_ndc": "68071-2267-1", "marketing_start_date": "20200924"}], "brand_name": "Ciprofloxacin", "product_id": "68071-2267_1d76786e-4b8e-9489-e063-6294a90a2a17", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "68071-2267", "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": "ANDA076794", "marketing_category": "ANDA", "marketing_start_date": "20061101", "listing_expiration_date": "20261231"}