Package 70518-0932-1

Brand: levofloxacin

Generic: levofloxacin
NDC Package

Package Facts

Identity

Package NDC 70518-0932-1
Digits Only 7051809321
Product NDC 70518-0932
Product ID 70518-0932_4847bcac-6557-1997-e063-6294a90a2328
Description

5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0932-1)

Marketing

Marketing Status
Marketed Since 2018-05-11
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": "4847bcac-6557-1997-e063-6294a90a2328", "openfda": {"nui": ["N0000193223", "M0372253"], "unii": ["6GNT3Y5LMF"], "rxcui": ["311296"], "spl_set_id": ["710c0c10-89a5-4954-8f74-acc187c5cf0f"], "pharm_class_cs": ["Fluoroquinolones [CS]"], "pharm_class_epc": ["Fluoroquinolone Antibacterial [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0932-1)", "package_ndc": "70518-0932-1", "marketing_start_date": "20180511"}], "brand_name": "Levofloxacin", "product_id": "70518-0932_4847bcac-6557-1997-e063-6294a90a2328", "dosage_form": "TABLET, FILM COATED", "product_ndc": "70518-0932", "generic_name": "Levofloxacin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levofloxacin", "active_ingredients": [{"name": "LEVOFLOXACIN", "strength": "750 mg/1"}], "application_number": "ANDA076710", "marketing_category": "ANDA", "marketing_start_date": "20180105", "listing_expiration_date": "20271231"}