Package 82804-260-14

Brand: ciprofloxacin hydrochloride

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82804-260-14
Digits Only 8280426014
Product NDC 82804-260
Product ID 82804-260_b281a5c0-5f3e-4e6f-86ac-ed7794aac64c
Description

14 TABLET, FILM COATED in 1 BOTTLE (82804-260-14)

Marketing

Marketing Status
Marketed Since 2025-12-30
Brand ciprofloxacin hydrochloride
Generic ciprofloxacin hydrochloride
Sample Package No

Linked Drug Pages (1)

Ciprofloxacin Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b281a5c0-5f3e-4e6f-86ac-ed7794aac64c", "openfda": {"upc": ["0382804260140"], "unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["b281a5c0-5f3e-4e6f-86ac-ed7794aac64c"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (82804-260-14)", "package_ndc": "82804-260-14", "marketing_start_date": "20251230"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (82804-260-20)", "package_ndc": "82804-260-20", "marketing_start_date": "20251230"}], "brand_name": "Ciprofloxacin Hydrochloride", "product_id": "82804-260_b281a5c0-5f3e-4e6f-86ac-ed7794aac64c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "82804-260", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin Hydrochloride", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA076593", "marketing_category": "ANDA", "marketing_start_date": "20240523", "listing_expiration_date": "20271231"}