Package 0409-4031-01

Brand: mannitol

Generic: mannitol
NDC Package

Package Facts

Identity

Package NDC 0409-4031-01
Digits Only 0409403101
Product NDC 0409-4031
Product ID 0409-4031_55985e1e-1dc4-4872-b2d6-c46db5338254
Description

25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4031-01) / 50 mL in 1 VIAL, SINGLE-DOSE (0409-4031-16)

Marketing

Marketing Status
Marketed Since 2004-11-30
Brand mannitol
Generic mannitol
Sample Package No

Linked Drug Pages (1)

Mannitol ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "55985e1e-1dc4-4872-b2d6-c46db5338254", "openfda": {"nui": ["N0000175359", "N0000010288", "N0000175810"], "unii": ["3OWL53L36A"], "rxcui": ["311450"], "spl_set_id": ["8ad3145e-00e7-4412-b9a5-06f00f264f30"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Osmotic Diuretic [EPC]"], "pharm_class_moa": ["Osmotic Activity [MoA]"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4031-01)  / 50 mL in 1 VIAL, SINGLE-DOSE (0409-4031-16)", "package_ndc": "0409-4031-01", "marketing_start_date": "20041130"}], "brand_name": "Mannitol", "product_id": "0409-4031_55985e1e-1dc4-4872-b2d6-c46db5338254", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis [PE]", "Osmotic Activity [MoA]", "Osmotic Diuretic [EPC]"], "product_ndc": "0409-4031", "generic_name": "MANNITOL", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mannitol", "active_ingredients": [{"name": "MANNITOL", "strength": "12.5 g/50mL"}], "application_number": "NDA016269", "marketing_category": "NDA", "marketing_start_date": "20041130", "listing_expiration_date": "20261231"}