Package 50090-7665-0

Brand: moxifloxacin hydrochloride

Generic: moxifloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7665-0
Digits Only 5009076650
Product NDC 50090-7665
Product ID 50090-7665_d5b39dfd-9893-4f07-955f-d3e476fa8fb8
Description

30 TABLET, FILM COATED in 1 BOTTLE (50090-7665-0)

Marketing

Marketing Status
Marketed Since 2025-10-01
Brand moxifloxacin hydrochloride
Generic moxifloxacin hydrochloride
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d5b39dfd-9893-4f07-955f-d3e476fa8fb8", "openfda": {"unii": ["C53598599T"], "rxcui": ["311787"], "spl_set_id": ["37466c79-8726-4fd6-9412-0bb83d523fe3"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-7665-0)", "package_ndc": "50090-7665-0", "marketing_start_date": "20251001"}], "brand_name": "Moxifloxacin Hydrochloride", "product_id": "50090-7665_d5b39dfd-9893-4f07-955f-d3e476fa8fb8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "50090-7665", "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"}