Package 63629-3257-1

Brand: desmopressin acetate

Generic: desmopressin acetate
NDC Package

Package Facts

Identity

Package NDC 63629-3257-1
Digits Only 6362932571
Product NDC 63629-3257
Description

90 TABLET in 1 BOTTLE (63629-3257-1)

Marketing

Marketing Status
Marketed Since 2024-10-10
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": "e6368593-40cc-4323-ac50-2aaa12b7a35d", "openfda": {"unii": ["XB13HYU18U"], "rxcui": ["833008"], "spl_set_id": ["dc9b0dad-d265-4dff-8191-d936280d85a2"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (63629-3257-1)", "package_ndc": "63629-3257-1", "marketing_start_date": "20241010"}], "brand_name": "Desmopressin Acetate", "product_id": "63629-3257_e6368593-40cc-4323-ac50-2aaa12b7a35d", "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": "63629-3257", "generic_name": "desmopressin acetate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desmopressin Acetate", "active_ingredients": [{"name": "DESMOPRESSIN ACETATE", "strength": ".2 mg/1"}], "application_number": "ANDA077414", "marketing_category": "ANDA", "marketing_start_date": "20060307", "listing_expiration_date": "20261231"}