Package 85293-002-01

Brand: ciprofloxacin

Generic: ciprofloxacin
NDC Package

Package Facts

Identity

Package NDC 85293-002-01
Digits Only 8529300201
Product NDC 85293-002
Product ID 85293-002_2fc39084-df93-4b13-e063-6394a90a38a8
Description

100 TABLET in 1 BOTTLE (85293-002-01)

Marketing

Marketing Status
Marketed Since 2025-03-05
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": "2fc39084-df93-4b13-e063-6394a90a38a8", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["197511", "197512", "309309"], "spl_set_id": ["0c355077-7361-41d0-9e82-eb31beaf5daa"], "manufacturer_name": ["Umasuto, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (85293-002-01)", "package_ndc": "85293-002-01", "marketing_start_date": "20250305"}], "brand_name": "ciprofloxacin", "product_id": "85293-002_2fc39084-df93-4b13-e063-6394a90a38a8", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "85293-002", "generic_name": "ciprofloxacin", "labeler_name": "Umasuto, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA076639", "marketing_category": "ANDA", "marketing_start_date": "20250305", "listing_expiration_date": "20261231"}