Package 70518-0719-0

Brand: levofloxacin

Generic: levofloxacin
NDC Package

Package Facts

Identity

Package NDC 70518-0719-0
Digits Only 7051807190
Product NDC 70518-0719
Product ID 70518-0719_48332f2b-f97c-f9fd-e063-6394a90affa8
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0719-0)

Marketing

Marketing Status
Marketed Since 2017-08-30
Brand levofloxacin
Generic levofloxacin
Sample Package No

Linked Drug Pages (1)

Levofloxacin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "48332f2b-f97c-f9fd-e063-6394a90affa8", "openfda": {"nui": ["N0000193223", "M0372253"], "unii": ["6GNT3Y5LMF"], "rxcui": ["199884"], "spl_set_id": ["b8ac5047-5203-42c4-886b-dd0b08a1786f"], "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 (70518-0719-0)", "package_ndc": "70518-0719-0", "marketing_start_date": "20170830"}], "brand_name": "Levofloxacin", "product_id": "70518-0719_48332f2b-f97c-f9fd-e063-6394a90affa8", "dosage_form": "TABLET, FILM COATED", "product_ndc": "70518-0719", "generic_name": "Levofloxacin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levofloxacin", "active_ingredients": [{"name": "LEVOFLOXACIN", "strength": "250 mg/1"}], "application_number": "ANDA202801", "marketing_category": "ANDA", "marketing_start_date": "20170830", "listing_expiration_date": "20271231"}