Package 80425-0239-1

Brand: moxifloxacin

Generic: moxifloxacin
NDC Package

Package Facts

Identity

Package NDC 80425-0239-1
Digits Only 8042502391
Product NDC 80425-0239
Product ID 80425-0239_2a9aa671-d0a2-2254-e063-6294a90a9f79
Description

1 BOTTLE, DROPPER in 1 CARTON (80425-0239-1) / 3 mL in 1 BOTTLE, DROPPER

Marketing

Marketing Status
Marketed Since 2023-01-11
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": "2a9aa671-d0a2-2254-e063-6294a90a9f79", "openfda": {"unii": ["B8956S8609"], "rxcui": ["403818"], "spl_set_id": ["f19fa89e-9f5d-4eed-e053-2995a90ac3ce"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (80425-0239-1)  / 3 mL in 1 BOTTLE, DROPPER", "package_ndc": "80425-0239-1", "marketing_start_date": "20230111"}], "brand_name": "Moxifloxacin", "product_id": "80425-0239_2a9aa671-d0a2-2254-e063-6294a90a9f79", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "80425-0239", "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": "ANDA090080", "marketing_category": "ANDA", "marketing_start_date": "20230111", "listing_expiration_date": "20261231"}