Package 31722-845-30

Brand: moxifloxacin

Generic: moxifloxacin
NDC Package

Package Facts

Identity

Package NDC 31722-845-30
Digits Only 3172284530
Product NDC 31722-845
Product ID 31722-845_40b874c7-8b88-6a93-e063-6394a90ad44f
Description

30 TABLET, FILM COATED in 1 BOTTLE (31722-845-30)

Marketing

Marketing Status
Marketed Since 2023-03-02
Brand moxifloxacin
Generic moxifloxacin
Sample Package No

Linked Drug Pages (1)

Moxifloxacin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "40b874c7-8b88-6a93-e063-6394a90ad44f", "openfda": {"upc": ["0331722845304"], "unii": ["C53598599T"], "rxcui": ["311787"], "spl_set_id": ["1e6bc886-eec9-4cd8-be78-7563817457f2"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (31722-845-05)", "package_ndc": "31722-845-05", "marketing_start_date": "20230302"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (31722-845-30)", "package_ndc": "31722-845-30", "marketing_start_date": "20230302"}], "brand_name": "Moxifloxacin", "product_id": "31722-845_40b874c7-8b88-6a93-e063-6394a90ad44f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "31722-845", "generic_name": "Moxifloxacin", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Moxifloxacin", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE", "strength": "400 mg/1"}], "application_number": "ANDA204836", "marketing_category": "ANDA", "marketing_start_date": "20230302", "listing_expiration_date": "20261231"}