Package 84549-024-25

Brand: mannitol

Generic: mannitol
NDC Package

Package Facts

Identity

Package NDC 84549-024-25
Digits Only 8454902425
Product NDC 84549-024
Product ID 84549-024_430669d7-9ad0-9a04-e063-6394a90ababb
Description

50 mL in 1 VIAL, SINGLE-DOSE (84549-024-25)

Marketing

Marketing Status
Marketed Since 2025-10-10
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": "430669d7-9ad0-9a04-e063-6394a90ababb", "openfda": {"nui": ["N0000175359", "N0000010288", "N0000175810"], "unii": ["3OWL53L36A"], "rxcui": ["311450"], "spl_set_id": ["430669d7-9ad1-9a04-e063-6394a90ababb"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Osmotic Diuretic [EPC]"], "pharm_class_moa": ["Osmotic Activity [MoA]"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 VIAL, SINGLE-DOSE (84549-024-25)", "package_ndc": "84549-024-25", "marketing_start_date": "20251010"}], "brand_name": "Mannitol", "product_id": "84549-024_430669d7-9ad0-9a04-e063-6394a90ababb", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis [PE]", "Osmotic Activity [MoA]", "Osmotic Diuretic [EPC]"], "product_ndc": "84549-024", "generic_name": "MANNITOL", "labeler_name": "ProPharma Distribution", "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"}