Package 82804-055-03

Brand: moxifloxacin

Generic: moxifloxacin
NDC Package

Package Facts

Identity

Package NDC 82804-055-03
Digits Only 8280405503
Product NDC 82804-055
Product ID 82804-055_c38e051f-5765-4066-9953-2d0832481b1e
Description

1 BOTTLE in 1 CARTON (82804-055-03) / 3 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2024-01-09
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": "c38e051f-5765-4066-9953-2d0832481b1e", "openfda": {"upc": ["0382804055036"], "unii": ["C53598599T"], "rxcui": ["403818"], "spl_set_id": ["c38e051f-5765-4066-9953-2d0832481b1e"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (82804-055-03)  / 3 mL in 1 BOTTLE", "package_ndc": "82804-055-03", "marketing_start_date": "20240109"}], "brand_name": "MOXIFLOXACIN", "product_id": "82804-055_c38e051f-5765-4066-9953-2d0832481b1e", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "82804-055", "generic_name": "MOXIFLOXACIN", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MOXIFLOXACIN", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA206242", "marketing_category": "ANDA", "marketing_start_date": "20171004", "listing_expiration_date": "20261231"}