mannitol

Generic: mannitol

Labeler: b. braun medical inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

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

mannitol 20 g/100mL

Manufacturer
B. Braun Medical Inc.

Identifiers & Regulatory

Product NDC 0264-7578
Product ID 0264-7578_33171b62-3532-4eb1-b273-714d07b0e3f8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA020006
Listing Expiration 2026-12-31
Marketing Start 1993-07-26

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 02647578
Hyphenated Format 0264-7578

Supplemental Identifiers

RxCUI
1791403 1791408
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 NDA020006 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 20 g/100mL
source: ndc
Packaging
  • 24 CONTAINER in 1 CASE (0264-7578-10) / 500 mL in 1 CONTAINER
  • 24 CONTAINER in 1 CASE (0264-7578-20) / 250 mL in 1 CONTAINER
source: ndc

Packages (2)

0264-7578-10 24 CONTAINER in 1 CASE (0264-7578-10) / 500 mL in 1 CONTAINER 0264-7578-20 24 CONTAINER in 1 CASE (0264-7578-20) / 250 mL in 1 CONTAINER

Ingredients (1)

mannitol (20 g/100mL)

Linked Drug Pages (1)

Mannitol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "33171b62-3532-4eb1-b273-714d07b0e3f8", "openfda": {"nui": ["N0000175359", "N0000010288", "N0000175810"], "unii": ["3OWL53L36A"], "rxcui": ["1791403", "1791408"], "spl_set_id": ["d12cc802-b538-4065-a264-f474ff3b3043"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Osmotic Diuretic [EPC]"], "pharm_class_moa": ["Osmotic Activity [MoA]"], "manufacturer_name": ["B. Braun Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 CONTAINER in 1 CASE (0264-7578-10)  / 500 mL in 1 CONTAINER", "package_ndc": "0264-7578-10", "marketing_start_date": "19930726"}, {"sample": false, "description": "24 CONTAINER in 1 CASE (0264-7578-20)  / 250 mL in 1 CONTAINER", "package_ndc": "0264-7578-20", "marketing_start_date": "19930726"}], "brand_name": "Mannitol", "product_id": "0264-7578_33171b62-3532-4eb1-b273-714d07b0e3f8", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis [PE]", "Osmotic Activity [MoA]", "Osmotic Diuretic [EPC]"], "product_ndc": "0264-7578", "generic_name": "MANNITOL", "labeler_name": "B. Braun Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mannitol", "active_ingredients": [{"name": "MANNITOL", "strength": "20 g/100mL"}], "application_number": "NDA020006", "marketing_category": "NDA", "marketing_start_date": "19930726", "listing_expiration_date": "20261231"}