Package 67457-323-25

Brand: moxifloxacin hydrochloride

Generic: moxifloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67457-323-25
Digits Only 6745732325
Product NDC 67457-323
Product ID 67457-323_c193663f-0749-4372-aab1-c43eb1b596e4
Description

1 BAG in 1 CARTON (67457-323-25) / 250 mL in 1 BAG

Marketing

Marketing Status
Marketed Since 2017-10-03
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": ["INTRAVENOUS"], "spl_id": "c193663f-0749-4372-aab1-c43eb1b596e4", "openfda": {"unii": ["C53598599T"], "rxcui": ["351156"], "spl_set_id": ["c6fa4129-2f92-4179-ac5d-bb7b4a538789"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BAG in 1 CARTON (67457-323-25)  / 250 mL in 1 BAG", "package_ndc": "67457-323-25", "marketing_start_date": "20171003"}], "brand_name": "MOXIFLOXACIN HYDROCHLORIDE", "product_id": "67457-323_c193663f-0749-4372-aab1-c43eb1b596e4", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "67457-323", "generic_name": "MOXIFLOXACIN HYDROCHLORIDE", "labeler_name": "Mylan Institutional LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MOXIFLOXACIN HYDROCHLORIDE", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE", "strength": "400 mg/250mL"}], "application_number": "ANDA205833", "marketing_category": "ANDA", "marketing_start_date": "20171003", "listing_expiration_date": "20271231"}