Package 63629-8357-2

Brand: moxifloxacin

Generic: moxifloxacin
NDC Package

Package Facts

Identity

Package NDC 63629-8357-2
Digits Only 6362983572
Product NDC 63629-8357
Description

10 TABLET, FILM COATED in 1 BOTTLE (63629-8357-2)

Marketing

Marketing Status
Marketed Since 2020-11-05
Brand moxifloxacin
Generic moxifloxacin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "27864513-a113-4ec1-9e78-41bc762172bc", "openfda": {"unii": ["C53598599T"], "rxcui": ["311787"], "spl_set_id": ["d20ba997-30de-445c-8766-924112bd834a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE (63629-8357-1)", "package_ndc": "63629-8357-1", "marketing_start_date": "20200917"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (63629-8357-2)", "package_ndc": "63629-8357-2", "marketing_start_date": "20201105"}], "brand_name": "Moxifloxacin", "product_id": "63629-8357_27864513-a113-4ec1-9e78-41bc762172bc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "63629-8357", "generic_name": "Moxifloxacin", "labeler_name": "Bryant Ranch Prepack", "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"}