Package 72843-459-10

Brand: desmopressin acetate

Generic: desmopressin acetate
NDC Package

Package Facts

Identity

Package NDC 72843-459-10
Digits Only 7284345910
Product NDC 72843-459
Description

10 AMPULE in 1 BOX (72843-459-10) / 1 mL in 1 AMPULE

Marketing

Marketing Status
Marketed Since 2020-02-14
Brand desmopressin acetate
Generic desmopressin acetate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "23150cfe-5244-9015-e063-6394a90aa7a4", "openfda": {"upc": ["0072843459109"], "unii": ["XB13HYU18U"], "rxcui": ["1723232"], "spl_set_id": ["b2fad59d-6176-4e09-9fbb-5cdd7f8f1568"], "manufacturer_name": ["UBI Pharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 AMPULE in 1 BOX (72843-459-10)  / 1 mL in 1 AMPULE", "package_ndc": "72843-459-10", "marketing_start_date": "20200214"}], "brand_name": "DESMOPRESSIN ACETATE", "product_id": "72843-459_23150cfe-5244-9015-e063-6394a90aa7a4", "dosage_form": "INJECTION", "pharm_class": ["Factor VIII Activator [EPC]", "Increased Coagulation Factor VIII Activity [PE]", "Increased Coagulation Factor VIII Concentration [PE]", "Vasopressin Analog [EPC]", "Vasopressins [CS]"], "product_ndc": "72843-459", "generic_name": "DESMOPRESSIN ACETATE", "labeler_name": "UBI Pharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DESMOPRESSIN ACETATE", "active_ingredients": [{"name": "DESMOPRESSIN ACETATE", "strength": "4 ug/mL"}], "application_number": "ANDA210218", "marketing_category": "ANDA", "marketing_start_date": "20200214", "listing_expiration_date": "20261231"}