Package 70518-0453-3

Brand: levofloxacin

Generic: levofloxacin
NDC Package

Package Facts

Identity

Package NDC 70518-0453-3
Digits Only 7051804533
Product NDC 70518-0453
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0453-3)

Marketing

Marketing Status
Marketed Since 2024-05-13
Brand levofloxacin
Generic levofloxacin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47f6f2fe-c984-3c24-e063-6294a90ac1cc", "openfda": {"nui": ["N0000193223", "M0372253"], "unii": ["6GNT3Y5LMF"], "rxcui": ["199885"], "spl_set_id": ["f14cf651-a213-4a4f-adb9-f628562af27c"], "pharm_class_cs": ["Fluoroquinolones [CS]"], "pharm_class_epc": ["Fluoroquinolone Antibacterial [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0453-3)", "package_ndc": "70518-0453-3", "marketing_start_date": "20240513"}], "brand_name": "Levofloxacin", "product_id": "70518-0453_47f6f2fe-c984-3c24-e063-6294a90ac1cc", "dosage_form": "TABLET, FILM COATED", "product_ndc": "70518-0453", "generic_name": "Levofloxacin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levofloxacin", "active_ingredients": [{"name": "LEVOFLOXACIN", "strength": "500 mg/1"}], "application_number": "ANDA076710", "marketing_category": "ANDA", "marketing_start_date": "20170421", "listing_expiration_date": "20271231"}