Package 16571-411-10

Brand: ciprofloxacin

Generic: ciprofloxacin
NDC Package

Package Facts

Identity

Package NDC 16571-411-10
Digits Only 1657141110
Product NDC 16571-411
Description

100 TABLET, FILM COATED in 1 BOTTLE (16571-411-10)

Marketing

Marketing Status
Marketed Since 2004-09-10
Brand ciprofloxacin
Generic ciprofloxacin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f031ce92-a4ed-45b0-8eb3-c3bdb02fbece", "openfda": {"upc": ["0316577411102", "0316571412501"], "unii": ["4BA73M5E37"], "rxcui": ["197511", "197512", "309309"], "spl_set_id": ["ef468722-68cd-440b-afd7-2285029db41f"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (16571-411-10)", "package_ndc": "16571-411-10", "marketing_start_date": "20040910"}], "brand_name": "ciprofloxacin", "product_id": "16571-411_f031ce92-a4ed-45b0-8eb3-c3bdb02fbece", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "16571-411", "generic_name": "ciprofloxacin", "labeler_name": "Rising Pharma Holdings, Inc.", "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": "20040910", "listing_expiration_date": "20261231"}