Package 50090-7244-1

Brand: moxifloxacin hydrochloride

Generic: moxifloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7244-1
Digits Only 5009072441
Product NDC 50090-7244
Product ID 50090-7244_54fdd364-609d-4d3a-8f62-8bc20bf3b74e
Description

7 TABLET, FILM COATED in 1 BOTTLE (50090-7244-1)

Marketing

Marketing Status
Marketed Since 2024-09-13
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": "54fdd364-609d-4d3a-8f62-8bc20bf3b74e", "openfda": {"unii": ["C53598599T"], "rxcui": ["311787"], "spl_set_id": ["02c29e8e-8346-4e28-b7fc-2f4cb61ad37d"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE (50090-7244-1)", "package_ndc": "50090-7244-1", "marketing_start_date": "20240913"}], "brand_name": "MOXIFLOXACIN HYDROCHLORIDE", "product_id": "50090-7244_54fdd364-609d-4d3a-8f62-8bc20bf3b74e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "50090-7244", "generic_name": "moxifloxacin hydrochloride", "labeler_name": "A-S Medication Solutions", "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": "20140304", "listing_expiration_date": "20261231"}