yutrepia
Generic: treprostinil
Labeler: liquidia technologies, inc.Drug Facts
Product Profile
Brand Name
yutrepia
Generic Name
treprostinil
Labeler
liquidia technologies, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
treprostinil sodium 53 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
72964-012
Product ID
72964-012_92c4515d-7de1-4bde-9ee9-f350696ba98d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA213005
Listing Expiration
2026-12-31
Marketing Start
2025-05-23
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72964012
Hyphenated Format
72964-012
Supplemental Identifiers
RxCUI
UNII
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
yutrepia (source: ndc)
Generic Name
treprostinil (source: ndc)
Application Number
NDA213005 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 53 ug/1
Packaging
- 7 BLISTER PACK in 1 CARTON (72964-012-01) / 4 CAPSULE in 1 BLISTER PACK / 1 CAPSULE in 1 CAPSULE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "92c4515d-7de1-4bde-9ee9-f350696ba98d", "openfda": {"unii": ["7JZ75N2NT6"], "rxcui": ["2714659", "2714664", "2714666", "2714668", "2714670", "2714672", "2714674", "2714676"], "spl_set_id": ["e8f6d534-115c-440e-bdbb-b443a29bb468"], "manufacturer_name": ["Liquidia Technologies, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "7 BLISTER PACK in 1 CARTON (72964-012-01) / 4 CAPSULE in 1 BLISTER PACK / 1 CAPSULE in 1 CAPSULE", "package_ndc": "72964-012-01", "marketing_start_date": "20250523"}], "brand_name": "Yutrepia", "product_id": "72964-012_92c4515d-7de1-4bde-9ee9-f350696ba98d", "dosage_form": "CAPSULE", "pharm_class": ["Prostacycline Vasodilator [EPC]", "Prostaglandins I [CS]", "Vasodilation [PE]"], "product_ndc": "72964-012", "generic_name": "treprostinil", "labeler_name": "Liquidia Technologies, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Yutrepia", "active_ingredients": [{"name": "TREPROSTINIL SODIUM", "strength": "53 ug/1"}], "application_number": "NDA213005", "marketing_category": "NDA", "marketing_start_date": "20250523", "listing_expiration_date": "20261231"}