Package 70095-026-02
Brand: desmopressin acetate
Generic: desmopressin acetatePackage Facts
Identity
Package NDC
70095-026-02
Digits Only
7009502602
Product NDC
70095-026
Description
10 VIAL, SINGLE-DOSE in 1 CARTON (70095-026-02) / 1 mL in 1 VIAL, SINGLE-DOSE (70095-026-01)
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": "353c7624-9af3-4103-9223-af53bc7371a5", "openfda": {"unii": ["XB13HYU18U"], "rxcui": ["1723232"], "spl_set_id": ["cdec2cc2-4fd9-474e-884f-d0599e40948f"], "manufacturer_name": ["Sun Pharmaceutical Industries Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (70095-026-02) / 1 mL in 1 VIAL, SINGLE-DOSE (70095-026-01)", "package_ndc": "70095-026-02", "marketing_start_date": "20230403"}], "brand_name": "Desmopressin Acetate", "product_id": "70095-026_353c7624-9af3-4103-9223-af53bc7371a5", "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": "70095-026", "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": "ANDA216922", "marketing_category": "ANDA", "marketing_start_date": "20230403", "listing_expiration_date": "20261231"}