Package 51662-1314-2
Brand: vasopressin
Generic: vasopressinPackage Facts
Identity
Package NDC
51662-1314-2
Digits Only
5166213142
Product NDC
51662-1314
Description
1 VIAL in 1 POUCH (51662-1314-2) / 1 mL in 1 VIAL
Marketing
Marketing Status
Brand
vasopressin
Generic
vasopressin
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "cfc4383a-4c3c-69a0-e053-2a95a90a268a", "openfda": {"unii": ["Y87Y826H08"], "rxcui": ["2103182"], "spl_set_id": ["7ae1c8c9-7d75-55a8-e053-2991aa0af05b"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL (51662-1314-1)", "package_ndc": "51662-1314-1", "marketing_start_date": "20181117"}, {"sample": false, "description": "1 VIAL in 1 POUCH (51662-1314-2) / 1 mL in 1 VIAL", "package_ndc": "51662-1314-2", "marketing_start_date": "20211101"}], "brand_name": "VASOPRESSIN", "product_id": "51662-1314_cfc4383a-4c3c-69a0-e053-2a95a90a268a", "dosage_form": "INJECTION", "product_ndc": "51662-1314", "generic_name": "VASOPRESSIN", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VASOPRESSIN", "active_ingredients": [{"name": "VASOPRESSIN, UNSPECIFIED", "strength": "20 [USP'U]/mL"}], "application_number": "NDA204485", "marketing_category": "NDA", "marketing_start_date": "20181117", "listing_expiration_date": "20261231"}