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FDA Approval

VASOPRESSIN

FDA-approved pharmaceutical product with comprehensive regulatory information, manufacturing details, and complete labeling documentation.

FDA Approval Summary

Company
Eugia US LLC
DUNS: 968961354
Effective Date
November 7, 2023
Labeling Type
Human Prescription Drug Label
Vasopressin(20 [USP'U] in 1 mL)

Manufacturing Establishments1

FDA-registered manufacturing facilities and establishments involved in the production, packaging, or distribution of this drug product.

Eugia Pharma Specialities Limited

Eugia US LLC

650498244

Products1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

VASOPRESSIN

Product Details

NDC Product Code
55150-370
Application Number
ANDA214314
Marketing Category
ANDA (C73584)
Route of Administration
INTRAVENOUS
Effective Date
November 7, 2023
CHLOROBUTANOLInactive
Code: HM4YQM8WRCClass: IACT
Code: Y87Y826H08Class: ACTIBQuantity: 20 [USP'U] in 1 mL
WATERInactive
Code: 059QF0KO0RClass: IACT
ACETIC ACIDInactive
Code: Q40Q9N063PClass: IACT
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