Package 72189-616-06

Brand: ciprofloxacin

Generic: ciprofloxacin
NDC Package

Package Facts

Identity

Package NDC 72189-616-06
Digits Only 7218961606
Product NDC 72189-616
Product ID 72189-616_2efbda2a-fc98-b7c5-e063-6294a90a362d
Description

6 TABLET in 1 BOTTLE (72189-616-06)

Marketing

Marketing Status
Marketed Since 2025-02-25
Brand ciprofloxacin
Generic ciprofloxacin
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": "2efbda2a-fc98-b7c5-e063-6294a90a362d", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["197511"], "spl_set_id": ["2efbda2a-fc97-b7c5-e063-6294a90a362d"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BOTTLE (72189-616-06)", "package_ndc": "72189-616-06", "marketing_start_date": "20250225"}], "brand_name": "Ciprofloxacin", "product_id": "72189-616_2efbda2a-fc98-b7c5-e063-6294a90a362d", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72189-616", "generic_name": "Ciprofloxacin", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA208921", "marketing_category": "ANDA", "marketing_start_date": "20250225", "listing_expiration_date": "20261231"}