Package 72189-242-20

Brand: ciprofloxacin

Generic: ciprofloxacin
NDC Package

Package Facts

Identity

Package NDC 72189-242-20
Digits Only 7218924220
Product NDC 72189-242
Description

20 TABLET, FILM COATED in 1 BOTTLE (72189-242-20)

Marketing

Marketing Status
Marketed Since 2021-07-23
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": "2c287767-b9e9-de36-e063-6394a90a5460", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["c7cea146-f179-5620-e053-2995a90acf83"], "manufacturer_name": ["direct rx"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (72189-242-10)", "package_ndc": "72189-242-10", "marketing_start_date": "20210723"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (72189-242-20)", "package_ndc": "72189-242-20", "marketing_start_date": "20210723"}], "brand_name": "CIPROFLOXACIN", "product_id": "72189-242_2c287767-b9e9-de36-e063-6394a90a5460", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72189-242", "generic_name": "CIPROFLOXACIN", "labeler_name": "direct rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CIPROFLOXACIN", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA075593", "marketing_category": "ANDA", "marketing_start_date": "20210723", "listing_expiration_date": "20261231"}