Package 66298-8507-4

Brand: moxifloxacin

Generic: moxifloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 66298-8507-4
Digits Only 6629885074
Product NDC 66298-8507
Product ID 66298-8507_1d783072-b073-e384-e063-6394a90a7460
Description

250 mL in 1 BAG (66298-8507-4)

Marketing

Marketing Status
Marketed Since 2017-08-02
Brand moxifloxacin
Generic moxifloxacin hydrochloride
Sample Package No

Linked Drug Pages (1)

Moxifloxacin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "1d783072-b073-e384-e063-6394a90a7460", "openfda": {"unii": ["C53598599T"], "rxcui": ["351156"], "spl_set_id": ["6067b2ee-2171-49bb-aa07-1d401ebf4f2e"], "manufacturer_name": ["Hp Halden Pharma AS"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "250 mL in 1 BAG (66298-8507-4)", "package_ndc": "66298-8507-4", "marketing_start_date": "20170802"}], "brand_name": "Moxifloxacin", "product_id": "66298-8507_1d783072-b073-e384-e063-6394a90a7460", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "66298-8507", "generic_name": "MOXIFLOXACIN HYDROCHLORIDE", "labeler_name": "Hp Halden Pharma AS", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Moxifloxacin", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE", "strength": "400 mg/250mL"}], "application_number": "NDA205572", "marketing_category": "NDA", "marketing_start_date": "20170802", "listing_expiration_date": "20261231"}