vasopressin

Generic: vasopressin

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name vasopressin
Generic Name vasopressin
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

vasopressin, unspecified 20 [USP'U]/mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1314
Product ID 51662-1314_cfc4383a-4c3c-69a0-e053-2a95a90a268a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA204485
Listing Expiration 2026-12-31
Marketing Start 2018-11-17

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621314
Hyphenated Format 51662-1314

Supplemental Identifiers

RxCUI
2103182
UNII
Y87Y826H08

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name vasopressin (source: ndc)
Generic Name vasopressin (source: ndc)
Application Number NDA204485 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 20 [USP'U]/mL
source: ndc
Packaging
  • 1 mL in 1 VIAL (51662-1314-1)
  • 1 VIAL in 1 POUCH (51662-1314-2) / 1 mL in 1 VIAL
source: ndc

Packages (2)

Ingredients (1)

vasopressin, unspecified (20 [USP'U]/mL)

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"}