Package 0404-9905-50
Brand: mannitol
Generic: mannitolPackage Facts
Identity
Package NDC
0404-9905-50
Digits Only
0404990550
Product NDC
0404-9905
Description
1 VIAL, SINGLE-DOSE in 1 BAG (0404-9905-50) / 50 mL in 1 VIAL, SINGLE-DOSE
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": "f3bb5de6-286d-4efc-a55d-e0b65dc4b1c2", "openfda": {"nui": ["N0000175359", "N0000010288", "N0000175810"], "unii": ["3OWL53L36A"], "rxcui": ["311450"], "spl_set_id": ["e2444db1-9dfe-451f-a33c-9b00786464d2"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Osmotic Diuretic [EPC]"], "pharm_class_moa": ["Osmotic Activity [MoA]"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BAG (0404-9905-50) / 50 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0404-9905-50", "marketing_start_date": "20220112"}], "brand_name": "Mannitol", "product_id": "0404-9905_f3bb5de6-286d-4efc-a55d-e0b65dc4b1c2", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis [PE]", "Osmotic Activity [MoA]", "Osmotic Diuretic [EPC]"], "product_ndc": "0404-9905", "generic_name": "Mannitol", "labeler_name": "Henry Schein, Inc.", "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": "20220112", "listing_expiration_date": "20261231"}