mannitol
Generic: mannitol
Labeler: icu medical inc.Drug Facts
Product Profile
Brand Name
mannitol
Generic Name
mannitol
Labeler
icu medical inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
mannitol 20 g/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
0990-7715
Product ID
0990-7715_b0dfadd1-70b5-49f5-8b63-60d3b4e1cbf5
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA019603
Listing Expiration
2026-12-31
Marketing Start
2019-05-31
Pharmacologic Class
Established (EPC)
Mechanism of Action
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
09907715
Hyphenated Format
0990-7715
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
NDA019603 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 g/100mL
Packaging
- 24 POUCH in 1 CASE (0990-7715-02) / 1 BAG in 1 POUCH / 250 mL in 1 BAG (0990-7715-12)
- 12 POUCH in 1 CASE (0990-7715-03) / 1 BAG in 1 POUCH / 500 mL in 1 BAG (0990-7715-13)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "b0dfadd1-70b5-49f5-8b63-60d3b4e1cbf5", "openfda": {"nui": ["N0000175359", "N0000010288", "N0000175810"], "unii": ["3OWL53L36A"], "rxcui": ["1791403", "1791408"], "spl_set_id": ["ba7bf864-8a4d-4262-8fd1-00174fa2f9d1"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Osmotic Diuretic [EPC]"], "pharm_class_moa": ["Osmotic Activity [MoA]"], "manufacturer_name": ["ICU Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 POUCH in 1 CASE (0990-7715-02) / 1 BAG in 1 POUCH / 250 mL in 1 BAG (0990-7715-12)", "package_ndc": "0990-7715-02", "marketing_start_date": "20190801"}, {"sample": false, "description": "12 POUCH in 1 CASE (0990-7715-03) / 1 BAG in 1 POUCH / 500 mL in 1 BAG (0990-7715-13)", "package_ndc": "0990-7715-03", "marketing_start_date": "20190531"}], "brand_name": "Mannitol", "product_id": "0990-7715_b0dfadd1-70b5-49f5-8b63-60d3b4e1cbf5", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis [PE]", "Osmotic Activity [MoA]", "Osmotic Diuretic [EPC]"], "product_ndc": "0990-7715", "generic_name": "MANNITOL", "labeler_name": "ICU Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mannitol", "active_ingredients": [{"name": "MANNITOL", "strength": "20 g/100mL"}], "application_number": "NDA019603", "marketing_category": "NDA", "marketing_start_date": "20190531", "listing_expiration_date": "20261231"}