Package 50090-4600-3

Brand: ciprofloxacin

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-4600-3
Digits Only 5009046003
Product NDC 50090-4600
Description

3 TABLET, FILM COATED in 1 BOTTLE (50090-4600-3)

Marketing

Marketing Status
Marketed Since 2019-10-11
Brand ciprofloxacin
Generic ciprofloxacin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "23da7d25-ba5c-4dcb-9351-e3ddfebdf614", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["197511"], "spl_set_id": ["6e37322b-89d3-4b66-8e1b-c4ad79eed173"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (50090-4600-0)", "package_ndc": "50090-4600-0", "marketing_start_date": "20191011"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (50090-4600-1)", "package_ndc": "50090-4600-1", "marketing_start_date": "20191011"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (50090-4600-2)", "package_ndc": "50090-4600-2", "marketing_start_date": "20191011"}, {"sample": false, "description": "3 TABLET, FILM COATED in 1 BOTTLE (50090-4600-3)", "package_ndc": "50090-4600-3", "marketing_start_date": "20191011"}], "brand_name": "Ciprofloxacin", "product_id": "50090-4600_23da7d25-ba5c-4dcb-9351-e3ddfebdf614", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "50090-4600", "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"}