Package 60505-0257-1
Brand: desmopressin acetate
Generic: desmopressin acetatePackage Facts
Identity
Package NDC
60505-0257-1
Digits Only
6050502571
Product NDC
60505-0257
Description
100 TABLET in 1 BOTTLE (60505-0257-1)
Marketing
Marketing Status
Brand
desmopressin acetate
Generic
desmopressin acetate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "41d13d8f-eeae-838d-fd10-bf7f568e903b", "openfda": {"unii": ["XB13HYU18U"], "rxcui": ["833008", "849515"], "spl_set_id": ["72aeef35-c102-b628-0219-9822651887eb"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (60505-0257-1)", "package_ndc": "60505-0257-1", "marketing_start_date": "20060307"}], "brand_name": "Desmopressin Acetate", "product_id": "60505-0257_41d13d8f-eeae-838d-fd10-bf7f568e903b", "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": "60505-0257", "generic_name": "desmopressin acetate", "labeler_name": "Apotex Corp.", "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": "20060307", "listing_expiration_date": "20261231"}