Package 72789-350-10

Brand: moxifloxacin hydrochloride

Generic: moxifloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-350-10
Digits Only 7278935010
Product NDC 72789-350
Product ID 72789-350_4bbf366b-77ca-fc66-e063-6394a90aebf4
Description

10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-350-10)

Marketing

Marketing Status
Marketed Since 2023-09-15
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": "4bbf366b-77ca-fc66-e063-6394a90aebf4", "openfda": {"upc": ["0372789350103"], "unii": ["C53598599T"], "rxcui": ["311787"], "spl_set_id": ["be5b7a6f-9ee3-4453-807e-4761fffff60c"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-350-10)", "package_ndc": "72789-350-10", "marketing_start_date": "20230915"}], "brand_name": "Moxifloxacin Hydrochloride", "product_id": "72789-350_4bbf366b-77ca-fc66-e063-6394a90aebf4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72789-350", "generic_name": "Moxifloxacin Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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": "20271231"}