Package 51655-327-84
Brand: levofloxacin
Generic: levofloxacinPackage Facts
Identity
Package NDC
51655-327-84
Digits Only
5165532784
Product NDC
51655-327
Description
14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-327-84)
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": "48eb0bd1-3a7e-3ba5-e063-6294a90a98c3", "openfda": {"nui": ["N0000193223", "M0372253"], "unii": ["6GNT3Y5LMF"], "rxcui": ["311296"], "spl_set_id": ["f2f090c2-3ee1-7689-e053-2995a90abe38"], "pharm_class_cs": ["Fluoroquinolones [CS]"], "pharm_class_epc": ["Fluoroquinolone Antibacterial [EPC]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-327-07)", "package_ndc": "51655-327-07", "marketing_start_date": "20230220"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-327-53)", "package_ndc": "51655-327-53", "marketing_start_date": "20230320"}, {"sample": false, "description": "5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-327-55)", "package_ndc": "51655-327-55", "marketing_start_date": "20221128"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-327-84)", "package_ndc": "51655-327-84", "marketing_start_date": "20240119"}], "brand_name": "Levofloxacin", "product_id": "51655-327_48eb0bd1-3a7e-3ba5-e063-6294a90a98c3", "dosage_form": "TABLET, FILM COATED", "product_ndc": "51655-327", "generic_name": "Levofloxacin", "labeler_name": "Northwind Health Company, LLC", "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": "20221128", "listing_expiration_date": "20271231"}