Package 80425-0379-1

Brand: moxifloxacin

Generic: moxifloxacin
NDC Package

Package Facts

Identity

Package NDC 80425-0379-1
Digits Only 8042503791
Product NDC 80425-0379
Product ID 80425-0379_14307586-424f-091a-e063-6394a90aee1f
Description

1 BOTTLE in 1 CARTON (80425-0379-1) / 3 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2024-03-21
Brand moxifloxacin
Generic moxifloxacin
Sample Package No

Linked Drug Pages (1)

Moxifloxacin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "14307586-424f-091a-e063-6394a90aee1f", "openfda": {"unii": ["B8956S8609"], "rxcui": ["403818"], "spl_set_id": ["143075b4-24d4-08a1-e063-6394a90a8a6e"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (80425-0379-1)  / 3 mL in 1 BOTTLE", "package_ndc": "80425-0379-1", "marketing_start_date": "20240321"}], "brand_name": "Moxifloxacin", "product_id": "80425-0379_14307586-424f-091a-e063-6394a90aee1f", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "80425-0379", "generic_name": "Moxifloxacin", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Moxifloxacin", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE", "strength": "5 mg/mL"}], "application_number": "ANDA202867", "marketing_category": "ANDA", "marketing_start_date": "20240321", "listing_expiration_date": "20261231"}