Package 82804-256-20

Brand: ciprofloxacin

Generic: ciprofolxacin
NDC Package

Package Facts

Identity

Package NDC 82804-256-20
Digits Only 8280425620
Product NDC 82804-256
Description

20 TABLET in 1 BOTTLE (82804-256-20)

Marketing

Marketing Status
Marketed Since 2025-12-18
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": "9f00ae9d-8707-4275-9eba-2ed72db8aea1", "openfda": {"upc": ["0382804256068"], "unii": ["4BA73M5E37"], "rxcui": ["197511"], "spl_set_id": ["9f00ae9d-8707-4275-9eba-2ed72db8aea1"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BOTTLE (82804-256-06)", "package_ndc": "82804-256-06", "marketing_start_date": "20251218"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (82804-256-20)", "package_ndc": "82804-256-20", "marketing_start_date": "20251218"}], "brand_name": "Ciprofloxacin", "product_id": "82804-256_9f00ae9d-8707-4275-9eba-2ed72db8aea1", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "82804-256", "generic_name": "Ciprofolxacin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA208921", "marketing_category": "ANDA", "marketing_start_date": "20231001", "listing_expiration_date": "20261231"}