Package 31722-721-50

Brand: levofloxacin

Generic: levofloxacin
NDC Package

Package Facts

Identity

Package NDC 31722-721-50
Digits Only 3172272150
Product NDC 31722-721
Description

50 TABLET, FILM COATED in 1 BOTTLE (31722-721-50)

Marketing

Marketing Status
Marketed Since 2015-01-09
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": "1fa0a846-34d8-d6f5-e063-6394a90a8e54", "openfda": {"nui": ["N0000193223", "M0372253"], "upc": ["0331722721509", "0331722723206"], "unii": ["6GNT3Y5LMF"], "rxcui": ["199884", "199885", "311296"], "spl_set_id": ["b43e9b51-568c-4d84-bbd1-d237120056c4"], "pharm_class_cs": ["Fluoroquinolones [CS]"], "pharm_class_epc": ["Fluoroquinolone Antibacterial [EPC]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BLISTER PACK (31722-721-31)", "package_ndc": "31722-721-31", "marketing_start_date": "20150109"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BLISTER PACK (31722-721-32)", "package_ndc": "31722-721-32", "marketing_start_date": "20150109"}, {"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE (31722-721-50)", "package_ndc": "31722-721-50", "marketing_start_date": "20150109"}], "brand_name": "Levofloxacin", "product_id": "31722-721_1fa0a846-34d8-d6f5-e063-6394a90a8e54", "dosage_form": "TABLET, FILM COATED", "product_ndc": "31722-721", "generic_name": "Levofloxacin", "labeler_name": "Camber Pharmaceuticals, 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": "20150109", "listing_expiration_date": "20261231"}