Package 60687-732-21

Brand: desmopressin acetate

Generic: desmopressin acetate
NDC Package

Package Facts

Identity

Package NDC 60687-732-21
Digits Only 6068773221
Product NDC 60687-732
Description

30 BLISTER PACK in 1 CARTON (60687-732-21) / 1 TABLET in 1 BLISTER PACK (60687-732-11)

Marketing

Marketing Status
Marketed Since 2023-12-28
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": "437dc780-8fd1-6205-e063-6394a90a19db", "openfda": {"unii": ["XB13HYU18U"], "rxcui": ["833008", "849515"], "spl_set_id": ["0d447b48-3f4b-430e-9e68-d8b9401c002e"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (60687-732-21)  / 1 TABLET in 1 BLISTER PACK (60687-732-11)", "package_ndc": "60687-732-21", "marketing_start_date": "20231228"}], "brand_name": "Desmopressin Acetate", "product_id": "60687-732_437dc780-8fd1-6205-e063-6394a90a19db", "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": "60687-732", "generic_name": "desmopressin acetate", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desmopressin Acetate", "active_ingredients": [{"name": "DESMOPRESSIN ACETATE", "strength": ".2 mg/1"}], "application_number": "ANDA077414", "marketing_category": "ANDA", "marketing_start_date": "20231228", "listing_expiration_date": "20261231"}