MedPath

Sterile Water

Sterile Water for Injection

Approved
Approval ID

3a6422e1-feee-4095-8883-2b0837039e6e

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Dec 16, 2024

Manufacturers
FDA

Hospira, Inc.

DUNS: 141588017

Products 1

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

WATER

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code0409-0024
Application NumberNDA018801
Product Classification
M
Marketing Category
C73594
G
Generic Name
WATER
Product Specifications
Route of AdministrationINTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Effective DateDecember 16, 2024
FDA Product Classification

INGREDIENTS (1)

WATERActive
Quantity: 1 mL in 1 mL
Code: 059QF0KO0R
Classification: ACTIB

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.

Sterile Water - FDA Drug Approval Details