Package 70518-4458-0

Brand: moxifloxacin hydrochloride

Generic: moxifloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4458-0
Digits Only 7051844580
Product NDC 70518-4458
Product ID 70518-4458_3d584177-4ca7-3709-e063-6394a90abdaa
Description

7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4458-0)

Marketing

Marketing Status
Marketed Since 2025-08-27
Brand moxifloxacin hydrochloride
Generic moxifloxacin hydrochloride
Sample Package No

Linked Drug Pages (1)

Moxifloxacin Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3d584177-4ca7-3709-e063-6394a90abdaa", "openfda": {"unii": ["C53598599T"], "rxcui": ["311787"], "spl_set_id": ["54377276-96bf-4140-9e90-55623ab6b013"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4458-0)", "package_ndc": "70518-4458-0", "marketing_start_date": "20250827"}], "brand_name": "Moxifloxacin Hydrochloride", "product_id": "70518-4458_3d584177-4ca7-3709-e063-6394a90abdaa", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "70518-4458", "generic_name": "Moxifloxacin Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Moxifloxacin Hydrochloride", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE", "strength": "400 mg/1"}], "application_number": "ANDA202632", "marketing_category": "ANDA", "marketing_start_date": "20250827", "listing_expiration_date": "20261231"}