Package 70518-4568-0
Brand: levofloxacin
Generic: levofloxacinPackage Facts
Identity
Package NDC
70518-4568-0
Digits Only
7051845680
Product NDC
70518-4568
Description
30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4568-0)
Marketing
Marketing Status
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": "4a141d5b-10b8-8f66-e063-6394a90a835e", "openfda": {"nui": ["N0000193223", "M0372253"], "unii": ["6GNT3Y5LMF"], "rxcui": ["199885"], "spl_set_id": ["264a3f71-f23e-45e3-926a-421bcccf4e3d"], "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 BLISTER PACK (70518-4568-0)", "package_ndc": "70518-4568-0", "marketing_start_date": "20260204"}], "brand_name": "levofloxacin", "product_id": "70518-4568_4a141d5b-10b8-8f66-e063-6394a90a835e", "dosage_form": "TABLET, FILM COATED", "product_ndc": "70518-4568", "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": "ANDA077652", "marketing_category": "ANDA", "marketing_start_date": "20260204", "listing_expiration_date": "20271231"}