72964-014 NDC - YUTREPIA (TREPROSTINIL)

Drug Information

  • Product NDC: 72964-014
  • Proprietary Name: Yutrepia
  • Non Proprietary Name: treprostinil
  • Active Ingredient(s): 106 ug/1 TREPROSTINIL SODIUM
  • Administration Route(s): RESPIRATORY (INHALATION)
  • Dosage Form(s): CAPSULE
  • Pharmacy Class(es): Prostacycline Vasodilator [EPC]; Prostaglandins I [CS]; Vasodilation [PE]

Labeler Information

Field Name Field Value
Labeler Name: Liquidia Technologies, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA213005
Marketing Category: NDA
Start Marketing Date:5/23/2025

Package Information

No. Package Code Package Description Billing Unit
172964-014-017 BLISTER PACK in 1 CARTON (72964-014-01) / 4 CAPSULE in 1 BLISTER PACK / 1 CAPSULE in 1 CAPSULE

NDC Record

Field Name Field Value Definition
PRODUCT NDC72964-014The 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 NAMEYutrepiaThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEtreprostinilThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMECAPSULEThe translation of the dosage form Code submitted by the firm.
ROUTE NAMERESPIRATORY (INHALATION)The translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE5/23/2025This 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 NUMBERNDA213005This 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 NAMELiquidia Technologies, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMETREPROSTINIL SODIUMAn 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 STRENGTH106 
ACTIVE INGRED UNITug/1 
PHARM CLASSESProstacycline Vasodilator [EPC], Prostaglandins I [CS], Vasodilation [PE] 

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This page was last updated on: 6/6/2025

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