Package 72843-461-10

Brand: desmopressin acetate

Generic: desmopressin acetate
NDC Package

Package Facts

Identity

Package NDC 72843-461-10
Digits Only 7284346110
Product NDC 72843-461
Description

10 VIAL in 1 CARTON (72843-461-10) / 1 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2020-09-17
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": "2e790f05-a105-6fda-e063-6294a90a146c", "openfda": {"upc": ["0072843440015"], "unii": ["XB13HYU18U"], "rxcui": ["849501", "1723232"], "spl_set_id": ["b01c22dc-eecd-11b2-e053-2a95a90a529a"], "manufacturer_name": ["UBI Pharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (72843-461-10)  / 1 mL in 1 VIAL", "package_ndc": "72843-461-10", "marketing_start_date": "20200917"}], "brand_name": "DESMOPRESSIN ACETATE", "product_id": "72843-461_2e790f05-a105-6fda-e063-6294a90a146c", "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": "72843-461", "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": "ANDA210223", "marketing_category": "ANDA", "marketing_start_date": "20200917", "listing_expiration_date": "20261231"}