vasopressin
Generic: vasopressin
Labeler: civica, inc.Drug Facts
Product Profile
Brand Name
vasopressin
Generic Name
vasopressin
Labeler
civica, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
vasopressin 20 [USP'U]/mL
Manufacturer
Identifiers & Regulatory
Product NDC
72572-860
Product ID
72572-860_5549bf12-c4f9-481d-a8bd-c8c75e439edb
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA212593
Listing Expiration
2026-12-31
Marketing Start
2025-10-22
Pharmacologic Class
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72572860
Hyphenated Format
72572-860
Supplemental Identifiers
RxCUI
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
NDA212593 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 [USP'U]/mL
Packaging
- 25 VIAL, SINGLE-DOSE in 1 CARTON (72572-860-25) / 1 mL in 1 VIAL, SINGLE-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "5549bf12-c4f9-481d-a8bd-c8c75e439edb", "openfda": {"nui": ["M0022562", "N0000009908", "N0000175360"], "unii": ["Y4907O6MFD"], "rxcui": ["2103182"], "spl_set_id": ["cce1a220-3178-49ec-b046-f0cb134cf051"], "pharm_class_cs": ["Vasopressins [CS]"], "pharm_class_pe": ["Vasoconstriction [PE]", "Decreased Diuresis [PE]"], "manufacturer_name": ["Civica, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (72572-860-25) / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "72572-860-25", "marketing_start_date": "20251022"}], "brand_name": "Vasopressin", "product_id": "72572-860_5549bf12-c4f9-481d-a8bd-c8c75e439edb", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Decreased Diuresis [PE]", "Vasoconstriction [PE]", "Vasopressins [CS]"], "product_ndc": "72572-860", "generic_name": "Vasopressin", "labeler_name": "Civica, 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": "20251022", "listing_expiration_date": "20261231"}