vasopressin
Generic: vasopressin
Labeler: fresenius kabi usa, llcDrug Facts
Product Profile
Brand Name
vasopressin
Generic Name
vasopressin
Labeler
fresenius kabi usa, llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
vasopressin 20 [USP'U]/mL
Manufacturer
Identifiers & Regulatory
Product NDC
65219-039
Product ID
65219-039_9fa80e75-4058-47f2-be6f-36d33062abd6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA213206
Listing Expiration
2026-12-31
Marketing Start
2023-05-26
Pharmacologic Class
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
65219039
Hyphenated Format
65219-039
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
ANDA213206 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 [USP'U]/mL
Packaging
- 25 VIAL, SINGLE-DOSE in 1 TRAY (65219-039-01) / 1 mL in 1 VIAL, SINGLE-DOSE (65219-039-00)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "9fa80e75-4058-47f2-be6f-36d33062abd6", "openfda": {"nui": ["M0022562", "N0000009908", "N0000175360"], "upc": ["0365219039006"], "unii": ["Y4907O6MFD"], "rxcui": ["2103182"], "spl_set_id": ["50aef1e8-0a70-466d-93cd-c1b9ed489839"], "pharm_class_cs": ["Vasopressins [CS]"], "pharm_class_pe": ["Vasoconstriction [PE]", "Decreased Diuresis [PE]"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (65219-039-01) / 1 mL in 1 VIAL, SINGLE-DOSE (65219-039-00)", "package_ndc": "65219-039-01", "marketing_start_date": "20230526"}], "brand_name": "VASOPRESSIN", "product_id": "65219-039_9fa80e75-4058-47f2-be6f-36d33062abd6", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Decreased Diuresis [PE]", "Vasoconstriction [PE]", "Vasopressins [CS]"], "product_ndc": "65219-039", "generic_name": "VASOPRESSIN", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VASOPRESSIN", "active_ingredients": [{"name": "VASOPRESSIN", "strength": "20 [USP'U]/mL"}], "application_number": "ANDA213206", "marketing_category": "ANDA", "marketing_start_date": "20230526", "listing_expiration_date": "20261231"}