Package 68001-574-00

Brand: desmopressin acetate

Generic: desmopressin acetate
NDC Package

Package Facts

Identity

Package NDC 68001-574-00
Digits Only 6800157400
Product NDC 68001-574
Description

100 TABLET in 1 BOTTLE (68001-574-00)

Marketing

Marketing Status
Marketed Since 2023-08-03
Brand desmopressin acetate
Generic desmopressin acetate
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "02150d95-2c55-cd5b-e063-6394a90aafad", "openfda": {"upc": ["0368001574006", "0368001575003"], "unii": ["XB13HYU18U"], "rxcui": ["833008", "849515"], "spl_set_id": ["c04357fd-478a-4909-b098-ae6710be071c"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68001-574-00)", "package_ndc": "68001-574-00", "marketing_start_date": "20230803"}], "brand_name": "Desmopressin Acetate", "product_id": "68001-574_02150d95-2c55-cd5b-e063-6394a90aafad", "dosage_form": "TABLET", "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": "68001-574", "generic_name": "desmopressin acetate", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desmopressin Acetate", "active_ingredients": [{"name": "DESMOPRESSIN ACETATE", "strength": ".1 mg/1"}], "application_number": "ANDA077414", "marketing_category": "ANDA", "marketing_start_date": "20230803", "listing_expiration_date": "20261231"}