Package 72162-2425-3

Brand: ciprofloxacin

Generic: ciprofolxacin
NDC Package

Package Facts

Identity

Package NDC 72162-2425-3
Digits Only 7216224253
Product NDC 72162-2425
Description

30 TABLET in 1 BOTTLE (72162-2425-3)

Marketing

Marketing Status
Marketed Since 2024-11-12
Brand ciprofloxacin
Generic ciprofolxacin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "54fb9efb-e34f-4d04-922b-c80eeb1c1200", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["ab16bacd-f73f-462e-82b2-b0abb1c49cec"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2425-1)", "package_ndc": "72162-2425-1", "marketing_start_date": "20241112"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (72162-2425-2)", "package_ndc": "72162-2425-2", "marketing_start_date": "20241112"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-2425-3)", "package_ndc": "72162-2425-3", "marketing_start_date": "20241112"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (72162-2425-4)", "package_ndc": "72162-2425-4", "marketing_start_date": "20241112"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72162-2425-5)", "package_ndc": "72162-2425-5", "marketing_start_date": "20241112"}], "brand_name": "Ciprofloxacin", "product_id": "72162-2425_54fb9efb-e34f-4d04-922b-c80eeb1c1200", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72162-2425", "generic_name": "Ciprofolxacin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA208921", "marketing_category": "ANDA", "marketing_start_date": "20231001", "listing_expiration_date": "20261231"}