Package 72964-012-01
Brand: yutrepia
Generic: treprostinilPackage Facts
Identity
Package NDC
72964-012-01
Digits Only
7296401201
Product NDC
72964-012
Description
7 BLISTER PACK in 1 CARTON (72964-012-01) / 4 CAPSULE in 1 BLISTER PACK / 1 CAPSULE in 1 CAPSULE
Marketing
Marketing Status
Brand
yutrepia
Generic
treprostinil
Sample Package
No
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"}