Package 69918-201-01
Brand: desmopressin acetate
Generic: desmopressin acetatePackage Facts
Identity
Package NDC
69918-201-01
Digits Only
6991820101
Product NDC
69918-201
Description
1 BOTTLE in 1 CARTON (69918-201-01) / 100 TABLET in 1 BOTTLE
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": ["ORAL"], "spl_id": "8f843a4f-10ba-4f8c-a86e-f599dbb7f322", "openfda": {"unii": ["XB13HYU18U"], "rxcui": ["833008", "849515"], "spl_set_id": ["c01048e8-d28f-4085-9c37-3d5d48395a77"], "manufacturer_name": ["Nordic Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (69918-201-01) / 100 TABLET in 1 BOTTLE", "package_ndc": "69918-201-01", "marketing_start_date": "20151210"}], "brand_name": "Desmopressin Acetate", "product_id": "69918-201_8f843a4f-10ba-4f8c-a86e-f599dbb7f322", "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": "69918-201", "generic_name": "Desmopressin Acetate", "labeler_name": "Nordic Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desmopressin Acetate", "active_ingredients": [{"name": "DESMOPRESSIN ACETATE", "strength": ".2 mg/1"}], "application_number": "NDA019955", "marketing_category": "NDA", "marketing_start_date": "20151210", "listing_expiration_date": "20261231"}