Package 80425-0164-1
Brand: ciprofloxacin
Generic: ciprofloxacinPackage Facts
Identity
Package NDC
80425-0164-1
Digits Only
8042501641
Product NDC
80425-0164
Description
20 TABLET, FILM COATED in 1 BOTTLE (80425-0164-1)
Marketing
Marketing Status
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": "2a99a670-af2f-299d-e063-6294a90a05d2", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["c8acca31-8d44-34a2-e053-2995a90ac20f"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (80425-0164-1)", "package_ndc": "80425-0164-1", "marketing_start_date": "20040609"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0164-2)", "package_ndc": "80425-0164-2", "marketing_start_date": "20040609"}], "brand_name": "Ciprofloxacin", "product_id": "80425-0164_2a99a670-af2f-299d-e063-6294a90a05d2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "80425-0164", "generic_name": "Ciprofloxacin", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA075593", "marketing_category": "ANDA", "marketing_start_date": "20040609", "listing_expiration_date": "20261231"}