Package 50090-7581-0

Brand: ciprofloxacin

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7581-0
Digits Only 5009075810
Product NDC 50090-7581
Product ID 50090-7581_c0735e0a-75d4-43f5-9be6-3508104d4142
Description

20 TABLET, FILM COATED in 1 BOTTLE (50090-7581-0)

Marketing

Marketing Status
Marketed Since 2025-06-16
Brand ciprofloxacin
Generic ciprofloxacin hydrochloride
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c0735e0a-75d4-43f5-9be6-3508104d4142", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["197511"], "spl_set_id": ["1dca6149-00ca-480e-a887-6861e40803b9"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (50090-7581-0)", "package_ndc": "50090-7581-0", "marketing_start_date": "20250616"}], "brand_name": "Ciprofloxacin", "product_id": "50090-7581_c0735e0a-75d4-43f5-9be6-3508104d4142", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "50090-7581", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA076126", "marketing_category": "ANDA", "marketing_start_date": "20091010", "listing_expiration_date": "20261231"}