vasopressin

Generic: vasopressin

Labeler: american regent, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name vasopressin
Generic Name vasopressin
Labeler american regent, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

vasopressin 20 [USP'U]/mL

Manufacturer
American Regent, Inc.

Identifiers & Regulatory

Product NDC 0517-1020
Product ID 0517-1020_36148e09-1c3c-4878-a194-8e10291972ff
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA212593
Listing Expiration 2026-12-31
Marketing Start 2022-02-03

Pharmacologic Class

Chemical Structure
vasopressins [cs]
Physiologic Effect
vasoconstriction [pe] decreased diuresis [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05171020
Hyphenated Format 0517-1020

Supplemental Identifiers

RxCUI
313578 2103182
UPC
0305171030017
UNII
Y4907O6MFD
NUI
M0022562 N0000009908 N0000175360

Packaging Origin

Original Packager
true

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 NDA212593 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 20 [USP'U]/mL
source: ndc
Packaging
  • 25 VIAL, SINGLE-DOSE in 1 CARTON (0517-1020-25) / 1 mL in 1 VIAL, SINGLE-DOSE (0517-1020-01)
source: ndc

Packages (1)

0517-1020-25 25 VIAL, SINGLE-DOSE in 1 CARTON (0517-1020-25) / 1 mL in 1 VIAL, SINGLE-DOSE (0517-1020-01)

Ingredients (1)

vasopressin (20 [USP'U]/mL)

Linked Drug Pages (1)

Vasopressin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "36148e09-1c3c-4878-a194-8e10291972ff", "openfda": {"nui": ["M0022562", "N0000009908", "N0000175360"], "upc": ["0305171030017"], "unii": ["Y4907O6MFD"], "rxcui": ["313578", "2103182"], "spl_set_id": ["0ab267f4-9ec9-44fd-8521-f975074667d9"], "pharm_class_cs": ["Vasopressins [CS]"], "pharm_class_pe": ["Vasoconstriction [PE]", "Decreased Diuresis [PE]"], "manufacturer_name": ["American Regent, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (0517-1020-25)  / 1 mL in 1 VIAL, SINGLE-DOSE (0517-1020-01)", "package_ndc": "0517-1020-25", "marketing_start_date": "20220203"}], "brand_name": "Vasopressin", "product_id": "0517-1020_36148e09-1c3c-4878-a194-8e10291972ff", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Decreased Diuresis [PE]", "Vasoconstriction [PE]", "Vasopressins [CS]"], "product_ndc": "0517-1020", "generic_name": "Vasopressin", "labeler_name": "American Regent, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vasopressin", "active_ingredients": [{"name": "VASOPRESSIN", "strength": "20 [USP'U]/mL"}], "application_number": "NDA212593", "marketing_category": "NDA", "marketing_start_date": "20220203", "listing_expiration_date": "20261231"}