Package 63323-850-04

Brand: moxifloxacin

Generic: moxifloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63323-850-04
Digits Only 6332385004
Product NDC 63323-850
Product ID 63323-850_4070f637-059f-4e3d-8cf3-e5256a46ff3e
Description

12 BAG in 1 CASE (63323-850-04) / 250 mL in 1 BAG (63323-850-74)

Marketing

Marketing Status
Marketed Since 2015-03-18
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": "4070f637-059f-4e3d-8cf3-e5256a46ff3e", "openfda": {"unii": ["C53598599T"], "rxcui": ["351156"], "spl_set_id": ["a4e28b09-714b-46e7-b4e6-0163cad78fc5"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 BAG in 1 CASE (63323-850-04)  / 250 mL in 1 BAG (63323-850-74)", "package_ndc": "63323-850-04", "marketing_start_date": "20150318"}], "brand_name": "Moxifloxacin", "product_id": "63323-850_4070f637-059f-4e3d-8cf3-e5256a46ff3e", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "63323-850", "generic_name": "MOXIFLOXACIN HYDROCHLORIDE", "labeler_name": "Fresenius Kabi USA, LLC", "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": "20150318", "listing_expiration_date": "20261231"}