Package 0338-0357-02

Brand: osmitrol

Generic: mannitol
NDC Package

Package Facts

Identity

Package NDC 0338-0357-02
Digits Only 0338035702
Product NDC 0338-0357
Description

250 mL in 1 BAG (0338-0357-02)

Marketing

Marketing Status
Marketed Since 1964-06-08
Brand osmitrol
Generic mannitol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "3911fd42-2b73-4509-9c4c-92ceba4e6d34", "openfda": {"nui": ["N0000175359", "N0000010288", "N0000175810"], "unii": ["3OWL53L36A"], "rxcui": ["206536", "1791395", "1791403", "1791404", "1791408", "1791409"], "spl_set_id": ["0d914965-7001-45cb-ba51-d7c5964b05bc"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Osmotic Diuretic [EPC]"], "pharm_class_moa": ["Osmotic Activity [MoA]"], "manufacturer_name": ["Baxter Healthcare Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "250 mL in 1 BAG (0338-0357-02)", "package_ndc": "0338-0357-02", "marketing_start_date": "19640608"}, {"sample": false, "description": "500 mL in 1 BAG (0338-0357-03)", "package_ndc": "0338-0357-03", "marketing_start_date": "19640608"}], "brand_name": "Osmitrol", "product_id": "0338-0357_3911fd42-2b73-4509-9c4c-92ceba4e6d34", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis [PE]", "Osmotic Activity [MoA]", "Osmotic Diuretic [EPC]"], "product_ndc": "0338-0357", "generic_name": "Mannitol", "labeler_name": "Baxter Healthcare Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Osmitrol", "active_ingredients": [{"name": "MANNITOL", "strength": "20 g/100mL"}], "application_number": "NDA013684", "marketing_category": "NDA", "marketing_start_date": "19640608", "listing_expiration_date": "20261231"}