Package 69117-0009-2

Brand: ciprofloxacin

Generic: ciprofloxacin tablets
NDC Package

Package Facts

Identity

Package NDC 69117-0009-2
Digits Only 6911700092
Product NDC 69117-0009
Description

100 TABLET, COATED in 1 BOTTLE (69117-0009-2)

Marketing

Marketing Status
Marketed Since 2019-07-13
Brand ciprofloxacin
Generic ciprofloxacin tablets
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47236eca-557e-1b27-e063-6394a90acd14", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["197511", "309309"], "spl_set_id": ["6fd3da0b-7428-ac8f-e053-2a91aa0aed9f"], "manufacturer_name": ["Yiling Pharmaceutical, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE (69117-0009-1)", "package_ndc": "69117-0009-1", "marketing_start_date": "20190713"}, {"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (69117-0009-2)", "package_ndc": "69117-0009-2", "marketing_start_date": "20190713"}], "brand_name": "Ciprofloxacin", "product_id": "69117-0009_47236eca-557e-1b27-e063-6394a90acd14", "dosage_form": "TABLET, COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "69117-0009", "generic_name": "Ciprofloxacin Tablets", "labeler_name": "Yiling Pharmaceutical, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA208921", "marketing_category": "ANDA", "marketing_start_date": "20190713", "listing_expiration_date": "20261231"}