Package 72843-440-01

Brand: desmopressin acetate

Generic: desmopressin acetate
NDC Package

Package Facts

Identity

Package NDC 72843-440-01
Digits Only 7284344001
Product NDC 72843-440
Description

1 VIAL in 1 CARTON (72843-440-01) / 10 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": "1 VIAL in 1 CARTON (72843-440-01)  / 10 mL in 1 VIAL", "package_ndc": "72843-440-01", "marketing_start_date": "20200917"}], "brand_name": "DESMOPRESSIN ACETATE", "product_id": "72843-440_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": "72843-440", "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": "40 ug/10mL"}], "application_number": "ANDA210223", "marketing_category": "ANDA", "marketing_start_date": "20200917", "listing_expiration_date": "20261231"}