Package 50090-1649-0

Brand: ciprofloxacin

Generic: ciprofloxacin
NDC Package

Package Facts

Identity

Package NDC 50090-1649-0
Digits Only 5009016490
Product NDC 50090-1649
Description

20 TABLET in 1 BOTTLE (50090-1649-0)

Marketing

Marketing Status
Marketed Since 2015-01-19
Brand ciprofloxacin
Generic ciprofloxacin
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9244d2d7-3da2-46a0-a870-9d1196df1504", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["6971a958-08f0-4712-bf5f-47fe4f76b863"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (50090-1649-0)", "package_ndc": "50090-1649-0", "marketing_start_date": "20150119"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (50090-1649-1)", "package_ndc": "50090-1649-1", "marketing_start_date": "20231031"}], "brand_name": "ciprofloxacin", "product_id": "50090-1649_9244d2d7-3da2-46a0-a870-9d1196df1504", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "50090-1649", "generic_name": "ciprofloxacin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA076639", "marketing_category": "ANDA", "marketing_start_date": "20040910", "listing_expiration_date": "20261231"}