vasopressin

Generic: vasopressin

Labeler: sagent pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name vasopressin
Generic Name vasopressin
Labeler sagent pharmaceuticals
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

vasopressin 20 [USP'U]/mL

Manufacturer
Sagent Pharmaceuticals

Identifiers & Regulatory

Product NDC 25021-474
Product ID 25021-474_c264bd5a-2111-48fc-8c43-1bd12d44006b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216963
Listing Expiration 2026-12-31
Marketing Start 2024-11-15

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 25021474
Hyphenated Format 25021-474

Supplemental Identifiers

RxCUI
2103182
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 ANDA216963 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 20 [USP'U]/mL
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (25021-474-01) / 1 mL in 1 VIAL
source: ndc

Packages (1)

25021-474-01 25 VIAL in 1 CARTON (25021-474-01) / 1 mL in 1 VIAL

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": "c264bd5a-2111-48fc-8c43-1bd12d44006b", "openfda": {"nui": ["M0022562", "N0000009908", "N0000175360"], "unii": ["Y4907O6MFD"], "rxcui": ["2103182"], "spl_set_id": ["ad3ac280-49da-4816-9097-14517d0c0f85"], "pharm_class_cs": ["Vasopressins [CS]"], "pharm_class_pe": ["Vasoconstriction [PE]", "Decreased Diuresis [PE]"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (25021-474-01)  / 1 mL in 1 VIAL", "package_ndc": "25021-474-01", "marketing_start_date": "20241115"}], "brand_name": "Vasopressin", "product_id": "25021-474_c264bd5a-2111-48fc-8c43-1bd12d44006b", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Decreased Diuresis [PE]", "Vasoconstriction [PE]", "Vasopressins [CS]"], "product_ndc": "25021-474", "generic_name": "Vasopressin", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vasopressin", "active_ingredients": [{"name": "VASOPRESSIN", "strength": "20 [USP'U]/mL"}], "application_number": "ANDA216963", "marketing_category": "ANDA", "marketing_start_date": "20241115", "listing_expiration_date": "20261231"}