Package 72789-085-50

Brand: levofloxacin

Generic: levofloxacin
NDC Package

Package Facts

Identity

Package NDC 72789-085-50
Digits Only 7278908550
Product NDC 72789-085
Description

50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-085-50)

Marketing

Marketing Status
Marketed Since 2020-06-16
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": "40319459-b17c-0929-e063-6294a90acf2f", "openfda": {"nui": ["N0000193223", "M0372253"], "upc": ["0372789085500"], "unii": ["6GNT3Y5LMF"], "rxcui": ["199885"], "spl_set_id": ["b8defac4-9deb-433b-928e-0ef4ee0123a2"], "pharm_class_cs": ["Fluoroquinolones [CS]"], "pharm_class_epc": ["Fluoroquinolone Antibacterial [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-085-50)", "package_ndc": "72789-085-50", "marketing_start_date": "20200616"}], "brand_name": "Levofloxacin", "product_id": "72789-085_40319459-b17c-0929-e063-6294a90acf2f", "dosage_form": "TABLET, FILM COATED", "product_ndc": "72789-085", "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"}