Package 72189-111-14

Brand: ciprofloxacin

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72189-111-14
Digits Only 7218911114
Product NDC 72189-111
Product ID 72189-111_4c499af5-b74b-2799-e063-6294a90a7054
Description

14 TABLET, FILM COATED in 1 BOTTLE (72189-111-14)

Marketing

Marketing Status
Discontinued 2027-02-28
Brand ciprofloxacin
Generic ciprofloxacin hydrochloride
Sample Package No

Linked Drug Pages (1)

CIPROFLOXACIN ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4c499af5-b74b-2799-e063-6294a90a7054", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["a7e5174a-dd01-6050-e053-2a95a90add3f"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (72189-111-10)", "package_ndc": "72189-111-10", "marketing_end_date": "20270228", "marketing_start_date": "20200612"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (72189-111-14)", "package_ndc": "72189-111-14", "marketing_end_date": "20270228", "marketing_start_date": "20200612"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (72189-111-20)", "package_ndc": "72189-111-20", "marketing_end_date": "20270228", "marketing_start_date": "20200612"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-111-30)", "package_ndc": "72189-111-30", "marketing_end_date": "20270228", "marketing_start_date": "20200612"}], "brand_name": "CIPROFLOXACIN", "product_id": "72189-111_4c499af5-b74b-2799-e063-6294a90a7054", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72189-111", "generic_name": "ciprofloxacin hydrochloride", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CIPROFLOXACIN", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA077859", "marketing_category": "ANDA", "marketing_end_date": "20270228", "marketing_start_date": "20200612"}