Package 0904-6353-61

Brand: levofloxacin

Generic: levofloxacin
NDC Package

Package Facts

Identity

Package NDC 0904-6353-61
Digits Only 0904635361
Product NDC 0904-6353
Description

100 BLISTER PACK in 1 CARTON (0904-6353-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2013-12-01
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": "7b6b4ee0-79a7-477b-bdc7-94111cc34ddb", "openfda": {"nui": ["N0000193223", "M0372253"], "unii": ["6GNT3Y5LMF"], "rxcui": ["199884", "199885", "311296"], "spl_set_id": ["ac4001ca-882f-4d9b-a570-c1b9d7fd6830"], "pharm_class_cs": ["Fluoroquinolones [CS]"], "pharm_class_epc": ["Fluoroquinolone Antibacterial [EPC]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6353-61)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6353-61", "marketing_start_date": "20131201"}], "brand_name": "Levofloxacin", "product_id": "0904-6353_7b6b4ee0-79a7-477b-bdc7-94111cc34ddb", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0904-6353", "generic_name": "Levofloxacin", "labeler_name": "Major Pharmaceuticals", "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": "20131201", "listing_expiration_date": "20261231"}