Package 65219-295-10

Brand: desmopressin acetate

Generic: desmopressin acetate
NDC Package

Package Facts

Identity

Package NDC 65219-295-10
Digits Only 6521929510
Product NDC 65219-295
Description

1 VIAL, MULTI-DOSE in 1 CARTON (65219-295-10) / 10 mL in 1 VIAL, MULTI-DOSE

Marketing

Marketing Status
Marketed Since 2023-09-11
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": "499d7fa7-43ab-47f0-ae4b-0f9791745f14", "openfda": {"unii": ["XB13HYU18U"], "rxcui": ["849501"], "spl_set_id": ["9725ba8e-ac0f-4655-bb98-9ea926142815"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (65219-295-10)  / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "65219-295-10", "marketing_start_date": "20230911"}], "brand_name": "Desmopressin Acetate", "product_id": "65219-295_499d7fa7-43ab-47f0-ae4b-0f9791745f14", "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": "65219-295", "generic_name": "Desmopressin Acetate", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desmopressin Acetate", "active_ingredients": [{"name": "DESMOPRESSIN ACETATE", "strength": "4 ug/mL"}], "application_number": "ANDA216904", "marketing_category": "ANDA", "marketing_start_date": "20230911", "listing_expiration_date": "20261231"}