Package 70095-031-01
Brand: desmopressin acetate
Generic: desmopressin acetatePackage Facts
Identity
Package NDC
70095-031-01
Digits Only
7009503101
Product NDC
70095-031
Description
1 VIAL in 1 CARTON (70095-031-01) / 10 mL in 1 VIAL
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": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "2a4f6931-2711-4831-8096-7acb266f4e22", "openfda": {"upc": ["0370095031013"], "unii": ["XB13HYU18U"], "rxcui": ["849501"], "spl_set_id": ["539d7da2-72b8-45f9-836c-4e3351dd488e"], "manufacturer_name": ["Sun Pharmaceutical Industries Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (70095-031-01) / 10 mL in 1 VIAL", "package_ndc": "70095-031-01", "marketing_start_date": "20230620"}], "brand_name": "Desmopressin Acetate", "product_id": "70095-031_2a4f6931-2711-4831-8096-7acb266f4e22", "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": "70095-031", "generic_name": "Desmopressin Acetate", "labeler_name": "Sun Pharmaceutical Industries Limited", "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": "20230620", "listing_expiration_date": "20261231"}