Sterile Water Injection
NDC Package 0409-4887-34
Package Information
Sterile Water (water) injection is this parenteral preparation is indicated only for diluting or dissolving drugs for intravenous, intramuscular or subcutaneous injection, according to instructions of the manufacturer of the drug to be administered. This formulation utilizes a injection delivery system. Marketed by Hospira, Inc., this product is identified by NDC 0409-4887 and is authorized under FDA application NDA018801.
Identification & Billing
Clinical Specifications
- Intramuscular - Administration within a muscle.
- Intravenous - Administration within or into a vein or veins.
- Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
Regulatory & Marketing
Hierarchy Structure
- 0409 - Hospira, Inc.
- 0409-4887 - Sterile Water
- 0409-4887-34 - 30 VIAL, PLASTIC in 1 TRAY / 10 mL in 1 VIAL, PLASTIC (0409-4887-32)
- 0409-4887 - Sterile Water
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
* Please review the full disclaimer at the bottom of this page.
Other Available Packages
The following commercial packages are registered under the same Product NDC (0409-4887). Click a package code to view its specific billing and regulatory data.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 0409-4887-34 identifies a specific commercial package of 30 vial, plastic in 1 tray / 10 ml in 1 vial, plastic (0409-4887-32) of Sterile Water, a human prescription drug labeled by Hospira, Inc.. This injection is formulated for intramuscular; intravenous; subcutaneous use and contains water as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Hospira, Inc. on June 16, 2005. The current certification is valid through December 31, 2027.
How is this Hospira, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00409488734. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Labeler segment to maintain the 5-4-2 structure.