vasopressin
Generic: vasopressin
Labeler: hf acquisition co llc, dba healthfirstDrug Facts
Product Profile
Brand Name
vasopressin
Generic Name
vasopressin
Labeler
hf acquisition co llc, dba healthfirst
Dosage Form
INJECTION
Routes
Active Ingredients
vasopressin, unspecified 20 [USP'U]/mL
Manufacturer
Identifiers & Regulatory
Product NDC
51662-1623
Product ID
51662-1623_39ae8951-80f9-e2c7-e063-6294a90a4f43
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA214314
Listing Expiration
2026-12-31
Marketing Start
2023-03-02
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621623
Hyphenated Format
51662-1623
Supplemental Identifiers
RxCUI
UNII
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
ANDA214314 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 [USP'U]/mL
Packaging
- 1 mL in 1 VIAL, MULTI-DOSE (51662-1623-1)
- 1 VIAL, MULTI-DOSE in 1 POUCH (51662-1623-2) / 1 mL in 1 VIAL, MULTI-DOSE
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "39ae8951-80f9-e2c7-e063-6294a90a4f43", "openfda": {"unii": ["Y87Y826H08"], "rxcui": ["313578"], "spl_set_id": ["f5f03364-e71c-9bcd-e053-2995a90a8ada"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL, MULTI-DOSE (51662-1623-1)", "package_ndc": "51662-1623-1", "marketing_start_date": "20230302"}, {"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 POUCH (51662-1623-2) / 1 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "51662-1623-2", "marketing_start_date": "20230302"}], "brand_name": "VASOPRESSIN", "product_id": "51662-1623_39ae8951-80f9-e2c7-e063-6294a90a4f43", "dosage_form": "INJECTION", "product_ndc": "51662-1623", "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": "ANDA214314", "marketing_category": "ANDA", "marketing_start_date": "20230302", "listing_expiration_date": "20261231"}