Package 55154-0193-0
Brand: ciprofloxacin
Generic: ciprofloxacinPackage Facts
Identity
Package NDC
55154-0193-0
Digits Only
5515401930
Product NDC
55154-0193
Description
10 BLISTER PACK in 1 BAG (55154-0193-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
ciprofloxacin
Generic
ciprofloxacin
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "922e9f5c-cc59-4d9e-bf42-a4b900d077ed", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["922e9f5c-cc59-4d9e-bf42-a4b900d077ed"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-0193-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "55154-0193-0", "marketing_start_date": "20251017"}], "brand_name": "ciprofloxacin", "product_id": "55154-0193_922e9f5c-cc59-4d9e-bf42-a4b900d077ed", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "55154-0193", "generic_name": "ciprofloxacin", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA076639", "marketing_category": "ANDA", "marketing_start_date": "20251017", "listing_expiration_date": "20261231"}