0990-7715 NDC - MANNITOL (MANNITOL)

Drug Information

Product NDC: 0990-7715

Proprietary Name: Mannitol

Non Proprietary Name: MANNITOL

Active Ingredient(s):
  • 20 g/100mL MANNITOL


Administration Route(s): INTRAVENOUS

Dosage Form(s): INJECTION, SOLUTION

Pharmacy Class(es):
  • Increased Diuresis [PE];
  • Osmotic Activity [MoA];
  • Osmotic Diuretic [EPC]

Labeler Information

Labeler Name: ICU Medical Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019603
Marketing Category: NDA
Start Marketing Date:5/31/2019

Package Information

No. Package Code Package Description Billing Unit
10990-7715-0224 POUCH in 1 CASE (0990-7715-02) / 1 BAG in 1 POUCH / 250 mL in 1 BAG (0990-7715-12)
20990-7715-0312 POUCH in 1 CASE (0990-7715-03) / 1 BAG in 1 POUCH / 500 mL in 1 BAG (0990-7715-13)ML

NDC Record

Field Name Field Value Definition
PRODUCT NDC0990-7715The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN PRESCRIPTION DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEMannitolThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEMANNITOLThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEINJECTION, SOLUTIONThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEINTRAVENOUSThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE5/31/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMENDAProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBERNDA019603This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMEICU Medical Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEMANNITOLAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH20 
ACTIVE INGRED UNITg/100mL 
PHARM CLASSESIncreased Diuresis [PE], Osmotic Activity [MoA], Osmotic Diuretic [EPC] 

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This page was last updated on: 2/1/2023