Package 80425-0499-1

Brand: ciprofloxacin

Generic: ciprofloxacin
NDC Package

Package Facts

Identity

Package NDC 80425-0499-1
Digits Only 8042504991
Product NDC 80425-0499
Description

1 BOTTLE, PLASTIC in 1 CARTON (80425-0499-1) / 5 mL in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2025-03-20
Brand ciprofloxacin
Generic ciprofloxacin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "30cb2b47-f440-5e22-e063-6294a90a8b3d", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309307"], "spl_set_id": ["30cb2b42-aa4b-8cec-e063-6394a90aa615"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (80425-0499-1)  / 5 mL in 1 BOTTLE, PLASTIC", "package_ndc": "80425-0499-1", "marketing_start_date": "20250320"}], "brand_name": "ciprofloxacin", "product_id": "80425-0499_30cb2b47-f440-5e22-e063-6294a90a8b3d", "dosage_form": "SOLUTION", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "80425-0499", "generic_name": "Ciprofloxacin", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "3 mg/mL"}], "application_number": "ANDA077568", "marketing_category": "ANDA", "marketing_start_date": "20250320", "listing_expiration_date": "20261231"}