Package 72189-300-06
Brand: ciprofloxacin
Generic: ciprofloxacinPackage Facts
Identity
Package NDC
72189-300-06
Digits Only
7218930006
Product NDC
72189-300
Description
6 TABLET, FILM COATED in 1 BOTTLE (72189-300-06)
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": "2c294bda-345b-ad0e-e063-6294a90a0304", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["d23e359d-6d12-38f6-e053-2a95a90a0a88"], "manufacturer_name": ["DirectRx"]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (72189-300-06)", "package_ndc": "72189-300-06", "marketing_start_date": "20211203"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (72189-300-20)", "package_ndc": "72189-300-20", "marketing_start_date": "20211203"}], "brand_name": "CIPROFLOXACIN", "product_id": "72189-300_2c294bda-345b-ad0e-e063-6294a90a0304", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72189-300", "generic_name": "CIPROFLOXACIN", "labeler_name": "DirectRx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CIPROFLOXACIN", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA076558", "marketing_category": "ANDA", "marketing_start_date": "20211203", "listing_expiration_date": "20261231"}