Package 71335-2342-1

Brand: desmopressin acetate

Generic: desmopressin acetate
NDC Package

Package Facts

Identity

Package NDC 71335-2342-1
Digits Only 7133523421
Product NDC 71335-2342
Product ID 71335-2342_c694f562-d5ea-468f-bccf-917437c5d606
Description

90 TABLET in 1 BOTTLE (71335-2342-1)

Marketing

Marketing Status
Marketed Since 2024-02-06
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": "c694f562-d5ea-468f-bccf-917437c5d606", "openfda": {"unii": ["XB13HYU18U"], "rxcui": ["833008"], "spl_set_id": ["52133714-37d1-458d-9839-f0bd206711ea"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2342-1)", "package_ndc": "71335-2342-1", "marketing_start_date": "20240206"}], "brand_name": "Desmopressin Acetate", "product_id": "71335-2342_c694f562-d5ea-468f-bccf-917437c5d606", "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": "71335-2342", "generic_name": "Desmopressin Acetate", "labeler_name": "Bryant Ranch Prepack", "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"}