Package 25021-461-10

Brand: desmopressin acetate

Generic: desmopressin acetate
NDC Package

Package Facts

Identity

Package NDC 25021-461-10
Digits Only 2502146110
Product NDC 25021-461
Description

1 VIAL in 1 CARTON (25021-461-10) / 10 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2018-03-15
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": "1d8f37fc-befe-491a-a90d-f24568660cca", "openfda": {"unii": ["XB13HYU18U"], "rxcui": ["849501"], "spl_set_id": ["40752c75-d09b-4013-9024-442048145b63"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (25021-461-10)  / 10 mL in 1 VIAL", "package_ndc": "25021-461-10", "marketing_start_date": "20180315"}], "brand_name": "desmopressin acetate", "product_id": "25021-461_1d8f37fc-befe-491a-a90d-f24568660cca", "dosage_form": "INJECTION, SOLUTION", "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": "25021-461", "generic_name": "desmopressin acetate", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "desmopressin acetate", "active_ingredients": [{"name": "DESMOPRESSIN ACETATE", "strength": "40 ug/10mL"}], "application_number": "ANDA204751", "marketing_category": "ANDA", "marketing_start_date": "20180315", "listing_expiration_date": "20261231"}