Package 50090-6609-1

Brand: moxifloxacin hydrochloride

Generic: moxifloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6609-1
Digits Only 5009066091
Product NDC 50090-6609
Product ID 50090-6609_20c49868-6dc2-4951-8729-16b51689c387
Description

7 TABLET, FILM COATED in 1 BOTTLE (50090-6609-1)

Marketing

Marketing Status
Marketed Since 2023-10-31
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": "20c49868-6dc2-4951-8729-16b51689c387", "openfda": {"unii": ["C53598599T"], "rxcui": ["311787"], "spl_set_id": ["c71e5987-edd7-4c38-b646-3e48a6e51bf4"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (50090-6609-0)", "package_ndc": "50090-6609-0", "marketing_start_date": "20230823"}, {"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE (50090-6609-1)", "package_ndc": "50090-6609-1", "marketing_start_date": "20231031"}], "brand_name": "Moxifloxacin Hydrochloride", "product_id": "50090-6609_20c49868-6dc2-4951-8729-16b51689c387", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "50090-6609", "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"}