Package 72789-367-07
Brand: levofloxacin
Generic: levofloxacinPackage Facts
Identity
Package NDC
72789-367-07
Digits Only
7278936707
Product NDC
72789-367
Description
7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-367-07)
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": "40bb6f48-ffba-c1e2-e063-6294a90af020", "openfda": {"nui": ["N0000193223", "M0372253"], "upc": ["0372789367071"], "unii": ["6GNT3Y5LMF"], "rxcui": ["199885"], "spl_set_id": ["b1a4aabb-42af-4133-8e82-0c7ec8fa79c3"], "pharm_class_cs": ["Fluoroquinolones [CS]"], "pharm_class_epc": ["Fluoroquinolone Antibacterial [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-367-07)", "package_ndc": "72789-367-07", "marketing_start_date": "20231211"}], "brand_name": "Levofloxacin", "product_id": "72789-367_40bb6f48-ffba-c1e2-e063-6294a90af020", "dosage_form": "TABLET, FILM COATED", "product_ndc": "72789-367", "generic_name": "Levofloxacin", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levofloxacin", "active_ingredients": [{"name": "LEVOFLOXACIN", "strength": "500 mg/1"}], "application_number": "ANDA201043", "marketing_category": "ANDA", "marketing_start_date": "20110620", "listing_expiration_date": "20261231"}