Package 63323-024-25

Brand: mannitol

Generic: mannitol
NDC Package

Package Facts

Identity

Package NDC 63323-024-25
Digits Only 6332302425
Product NDC 63323-024
Product ID 63323-024_fe8beed4-a8db-400e-834e-b5efe2f5af1c
Description

25 VIAL, SINGLE-DOSE in 1 TRAY (63323-024-25) / 50 mL in 1 VIAL, SINGLE-DOSE (63323-024-01)

Marketing

Marketing Status
Marketed Since 2000-03-19
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": "fe8beed4-a8db-400e-834e-b5efe2f5af1c", "openfda": {"nui": ["N0000175359", "N0000010288", "N0000175810"], "upc": ["0363323024017"], "unii": ["3OWL53L36A"], "rxcui": ["311450"], "spl_set_id": ["c395e13d-6ea1-4104-8b37-669cfb982f04"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Osmotic Diuretic [EPC]"], "pharm_class_moa": ["Osmotic Activity [MoA]"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (63323-024-25)  / 50 mL in 1 VIAL, SINGLE-DOSE (63323-024-01)", "package_ndc": "63323-024-25", "marketing_start_date": "20000319"}], "brand_name": "Mannitol", "product_id": "63323-024_fe8beed4-a8db-400e-834e-b5efe2f5af1c", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis [PE]", "Osmotic Activity [MoA]", "Osmotic Diuretic [EPC]"], "product_ndc": "63323-024", "generic_name": "MANNITOL", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mannitol", "active_ingredients": [{"name": "MANNITOL", "strength": "250 mg/mL"}], "application_number": "ANDA080677", "marketing_category": "ANDA", "marketing_start_date": "20000319", "listing_expiration_date": "20261231"}