Package 0264-7578-10

Brand: mannitol

Generic: mannitol
NDC Package

Package Facts

Identity

Package NDC 0264-7578-10
Digits Only 0264757810
Product NDC 0264-7578
Description

24 CONTAINER in 1 CASE (0264-7578-10) / 500 mL in 1 CONTAINER

Marketing

Marketing Status
Marketed Since 1993-07-26
Brand mannitol
Generic mannitol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "33171b62-3532-4eb1-b273-714d07b0e3f8", "openfda": {"nui": ["N0000175359", "N0000010288", "N0000175810"], "unii": ["3OWL53L36A"], "rxcui": ["1791403", "1791408"], "spl_set_id": ["d12cc802-b538-4065-a264-f474ff3b3043"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Osmotic Diuretic [EPC]"], "pharm_class_moa": ["Osmotic Activity [MoA]"], "manufacturer_name": ["B. Braun Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 CONTAINER in 1 CASE (0264-7578-10)  / 500 mL in 1 CONTAINER", "package_ndc": "0264-7578-10", "marketing_start_date": "19930726"}, {"sample": false, "description": "24 CONTAINER in 1 CASE (0264-7578-20)  / 250 mL in 1 CONTAINER", "package_ndc": "0264-7578-20", "marketing_start_date": "19930726"}], "brand_name": "Mannitol", "product_id": "0264-7578_33171b62-3532-4eb1-b273-714d07b0e3f8", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis [PE]", "Osmotic Activity [MoA]", "Osmotic Diuretic [EPC]"], "product_ndc": "0264-7578", "generic_name": "MANNITOL", "labeler_name": "B. Braun Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mannitol", "active_ingredients": [{"name": "MANNITOL", "strength": "20 g/100mL"}], "application_number": "NDA020006", "marketing_category": "NDA", "marketing_start_date": "19930726", "listing_expiration_date": "20261231"}