Package 59651-249-01

Brand: desmopressin acetate

Generic: desmopressin acetate
NDC Package

Package Facts

Identity

Package NDC 59651-249-01
Digits Only 5965124901
Product NDC 59651-249
Description

100 TABLET in 1 BOTTLE (59651-249-01)

Marketing

Marketing Status
Marketed Since 2024-03-21
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": "24866ad0-94db-46a2-96c0-b362acd0271a", "openfda": {"unii": ["XB13HYU18U"], "rxcui": ["833008", "849515"], "spl_set_id": ["24866ad0-94db-46a2-96c0-b362acd0271a"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (59651-249-01)", "package_ndc": "59651-249-01", "marketing_start_date": "20240321"}], "brand_name": "Desmopressin Acetate", "product_id": "59651-249_24866ad0-94db-46a2-96c0-b362acd0271a", "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": "59651-249", "generic_name": "desmopressin acetate", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desmopressin Acetate", "active_ingredients": [{"name": "DESMOPRESSIN ACETATE", "strength": ".1 mg/1"}], "application_number": "ANDA213095", "marketing_category": "ANDA", "marketing_start_date": "20240321", "listing_expiration_date": "20261231"}