Package 51662-1468-1
Brand: mannitol
Generic: mannitolPackage Facts
Identity
Package NDC
51662-1468-1
Digits Only
5166214681
Product NDC
51662-1468
Description
50 mL in 1 VIAL, SINGLE-DOSE (51662-1468-1)
Marketing
Marketing Status
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": "0ffaf004-4d61-3fd4-e063-6294a90a1a63", "openfda": {"nui": ["N0000175359", "N0000010288", "N0000175810"], "unii": ["3OWL53L36A"], "rxcui": ["311450"], "spl_set_id": ["999ce711-2d5b-0d7d-e053-2995a90a2689"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Osmotic Diuretic [EPC]"], "pharm_class_moa": ["Osmotic Activity [MoA]"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 VIAL, SINGLE-DOSE (51662-1468-1)", "package_ndc": "51662-1468-1", "marketing_start_date": "20191213"}, {"sample": false, "description": "25 POUCH in 1 CASE (51662-1468-3) / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1468-2) / 50 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "51662-1468-3", "marketing_start_date": "20221211"}], "brand_name": "MANNITOL", "product_id": "51662-1468_0ffaf004-4d61-3fd4-e063-6294a90a1a63", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis [PE]", "Osmotic Activity [MoA]", "Osmotic Diuretic [EPC]"], "product_ndc": "51662-1468", "generic_name": "MANNITOL", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "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": "20191213", "listing_expiration_date": "20261231"}