Package 72789-233-10

Brand: moxifloxacin

Generic: moxifloxacin
NDC Package

Package Facts

Identity

Package NDC 72789-233-10
Digits Only 7278923310
Product NDC 72789-233
Product ID 72789-233_40ad11b9-8248-8d3f-e063-6294a90a26eb
Description

10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-233-10)

Marketing

Marketing Status
Marketed Since 2022-02-15
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": "40ad11b9-8248-8d3f-e063-6294a90a26eb", "openfda": {"upc": ["0372789233109"], "unii": ["C53598599T"], "rxcui": ["311787"], "spl_set_id": ["1c6f7150-a8f4-408f-956f-c26d37030cf4"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-233-10)", "package_ndc": "72789-233-10", "marketing_start_date": "20220215"}], "brand_name": "Moxifloxacin", "product_id": "72789-233_40ad11b9-8248-8d3f-e063-6294a90a26eb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72789-233", "generic_name": "Moxifloxacin", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Moxifloxacin", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE", "strength": "400 mg/1"}], "application_number": "ANDA076938", "marketing_category": "ANDA", "marketing_start_date": "20140305", "listing_expiration_date": "20261231"}