Package 71205-234-90
Brand: levofloxacin
Generic: levofloxacinPackage Facts
Identity
Package NDC
71205-234-90
Digits Only
7120523490
Product NDC
71205-234
Description
90 TABLET, FILM COATED in 1 BOTTLE (71205-234-90)
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": "1d9c3263-38b0-47a4-ba6f-f553254fc442", "openfda": {"nui": ["N0000193223", "M0372253"], "upc": ["0371205234072"], "unii": ["6GNT3Y5LMF"], "rxcui": ["311296"], "spl_set_id": ["960fabb4-6156-4600-9a0f-7c24a89e9a31"], "pharm_class_cs": ["Fluoroquinolones [CS]"], "pharm_class_epc": ["Fluoroquinolone Antibacterial [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "5 TABLET, FILM COATED in 1 BOTTLE (71205-234-05)", "package_ndc": "71205-234-05", "marketing_start_date": "20190301"}, {"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE (71205-234-07)", "package_ndc": "71205-234-07", "marketing_start_date": "20190301"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (71205-234-10)", "package_ndc": "71205-234-10", "marketing_start_date": "20190301"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (71205-234-15)", "package_ndc": "71205-234-15", "marketing_start_date": "20190301"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-234-30)", "package_ndc": "71205-234-30", "marketing_start_date": "20190301"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-234-60)", "package_ndc": "71205-234-60", "marketing_start_date": "20190301"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-234-90)", "package_ndc": "71205-234-90", "marketing_start_date": "20190301"}], "brand_name": "Levofloxacin", "product_id": "71205-234_1d9c3263-38b0-47a4-ba6f-f553254fc442", "dosage_form": "TABLET, FILM COATED", "product_ndc": "71205-234", "generic_name": "Levofloxacin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levofloxacin", "active_ingredients": [{"name": "LEVOFLOXACIN", "strength": "750 mg/1"}], "application_number": "ANDA200839", "marketing_category": "ANDA", "marketing_start_date": "20120322", "listing_expiration_date": "20261231"}