Package 62756-529-40
Brand: desmopressin acetate
Generic: desmopressin acetatePackage Facts
Identity
Package NDC
62756-529-40
Digits Only
6275652940
Product NDC
62756-529
Description
1 VIAL in 1 CARTON (62756-529-40) / 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": "ec29b269-1ce9-4199-ab07-a51d3e55d604", "openfda": {"upc": ["0362756529403"], "unii": ["XB13HYU18U"], "rxcui": ["849501"], "spl_set_id": ["9fd48eec-aa24-4888-b99f-d409ada958a7"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (62756-529-40) / 10 mL in 1 VIAL", "package_ndc": "62756-529-40", "marketing_start_date": "20130130"}], "brand_name": "Desmopressin Acetate", "product_id": "62756-529_ec29b269-1ce9-4199-ab07-a51d3e55d604", "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": "62756-529", "generic_name": "Desmopressin Acetate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desmopressin Acetate", "active_ingredients": [{"name": "DESMOPRESSIN ACETATE", "strength": "4 ug/mL"}], "application_number": "ANDA091280", "marketing_category": "ANDA", "marketing_start_date": "20130130", "listing_expiration_date": "20261231"}