Package 10702-169-01

Brand: desmopressin acetate

Generic: desmopressin acetate
NDC Package

Package Facts

Identity

Package NDC 10702-169-01
Digits Only 1070216901
Product NDC 10702-169
Product ID 10702-169_11e764a6-0d02-ec11-e063-6394a90a195e
Description

100 TABLET in 1 BOTTLE (10702-169-01)

Marketing

Marketing Status
Marketed Since 2019-01-28
Brand desmopressin acetate
Generic desmopressin acetate
Sample Package No

Linked Drug Pages (1)

Desmopressin Acetate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "11e764a6-0d02-ec11-e063-6394a90a195e", "openfda": {"unii": ["XB13HYU18U"], "rxcui": ["833008", "849515"], "spl_set_id": ["9fba5e90-f541-4588-a5e9-b56198f17e87"], "manufacturer_name": ["KVK-TECH, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (10702-169-01)", "package_ndc": "10702-169-01", "marketing_start_date": "20190128"}], "brand_name": "Desmopressin Acetate", "product_id": "10702-169_11e764a6-0d02-ec11-e063-6394a90a195e", "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": "10702-169", "generic_name": "Desmopressin Acetate", "labeler_name": "KVK-TECH, INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desmopressin Acetate", "active_ingredients": [{"name": "DESMOPRESSIN ACETATE", "strength": ".1 mg/1"}], "application_number": "ANDA210371", "marketing_category": "ANDA", "marketing_start_date": "20190128", "listing_expiration_date": "20261231"}