mannitol

Generic: mannitol

Labeler: hospira, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name mannitol
Generic Name mannitol
Labeler hospira, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

mannitol 12.5 g/50mL

Manufacturer
Hospira, Inc.

Identifiers & Regulatory

Product NDC 0409-4031
Product ID 0409-4031_55985e1e-1dc4-4872-b2d6-c46db5338254
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA016269
Listing Expiration 2026-12-31
Marketing Start 2004-11-30

Pharmacologic Class

Established (EPC)
osmotic diuretic [epc]
Mechanism of Action
osmotic activity [moa]
Physiologic Effect
increased diuresis [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04094031
Hyphenated Format 0409-4031

Supplemental Identifiers

RxCUI
311450
UNII
3OWL53L36A
NUI
N0000175359 N0000010288 N0000175810

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name mannitol (source: ndc)
Generic Name mannitol (source: ndc)
Application Number NDA016269 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 12.5 g/50mL
source: ndc
Packaging
  • 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4031-01) / 50 mL in 1 VIAL, SINGLE-DOSE (0409-4031-16)
source: ndc

Packages (1)

0409-4031-01 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4031-01) / 50 mL in 1 VIAL, SINGLE-DOSE (0409-4031-16)

Ingredients (1)

mannitol (12.5 g/50mL)

Linked Drug Pages (1)

Mannitol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "55985e1e-1dc4-4872-b2d6-c46db5338254", "openfda": {"nui": ["N0000175359", "N0000010288", "N0000175810"], "unii": ["3OWL53L36A"], "rxcui": ["311450"], "spl_set_id": ["8ad3145e-00e7-4412-b9a5-06f00f264f30"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Osmotic Diuretic [EPC]"], "pharm_class_moa": ["Osmotic Activity [MoA]"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4031-01)  / 50 mL in 1 VIAL, SINGLE-DOSE (0409-4031-16)", "package_ndc": "0409-4031-01", "marketing_start_date": "20041130"}], "brand_name": "Mannitol", "product_id": "0409-4031_55985e1e-1dc4-4872-b2d6-c46db5338254", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis [PE]", "Osmotic Activity [MoA]", "Osmotic Diuretic [EPC]"], "product_ndc": "0409-4031", "generic_name": "MANNITOL", "labeler_name": "Hospira, 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": "20041130", "listing_expiration_date": "20261231"}