Package 80425-0493-2

Brand: ciprofloxacin hydrochloride

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 80425-0493-2
Digits Only 8042504932
Product NDC 80425-0493
Product ID 80425-0493_30caad43-7ca1-c06c-e063-6294a90afdeb
Description

30 TABLET, FILM COATED in 1 BOTTLE (80425-0493-2)

Marketing

Marketing Status
Marketed Since 2025-03-20
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": "30caad43-7ca1-c06c-e063-6294a90afdeb", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["30caadee-3255-e0e3-e063-6294a90a8061"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (80425-0493-1)", "package_ndc": "80425-0493-1", "marketing_start_date": "20250320"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0493-2)", "package_ndc": "80425-0493-2", "marketing_start_date": "20250320"}], "brand_name": "Ciprofloxacin Hydrochloride", "product_id": "80425-0493_30caad43-7ca1-c06c-e063-6294a90afdeb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "80425-0493", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "Advanced Rx of Tennessee, LLC", "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": "20250320", "listing_expiration_date": "20261231"}