Package 51655-461-52

Brand: desmopressin acetate

Generic: desmopressin acetate
NDC Package

Package Facts

Identity

Package NDC 51655-461-52
Digits Only 5165546152
Product NDC 51655-461
Product ID 51655-461_490efdbc-280a-2644-e063-6294a90a583d
Description

30 TABLET in 1 BOTTLE, PLASTIC (51655-461-52)

Marketing

Marketing Status
Marketed Since 2020-10-29
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": "490efdbc-280a-2644-e063-6294a90a583d", "openfda": {"unii": ["XB13HYU18U"], "rxcui": ["833008"], "spl_set_id": ["f306e2d4-781f-ff8f-e053-2a95a90ad15b"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-461-52)", "package_ndc": "51655-461-52", "marketing_start_date": "20201029"}], "brand_name": "Desmopressin Acetate", "product_id": "51655-461_490efdbc-280a-2644-e063-6294a90a583d", "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": "51655-461", "generic_name": "Desmopressin Acetate", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desmopressin Acetate", "active_ingredients": [{"name": "DESMOPRESSIN ACETATE", "strength": ".2 mg/1"}], "application_number": "ANDA210371", "marketing_category": "ANDA", "marketing_start_date": "20201029", "listing_expiration_date": "20271231"}