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  5. NDC Package Code: 0409-4887-34 Sterile Water

NDC Package 0409-4887-34 Sterile Water

Water Injection Intramuscular; Intravenous; Subcutaneous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
0409-4887-34
Package Description:
30 VIAL, PLASTIC in 1 TRAY / 10 mL in 1 VIAL, PLASTIC (0409-4887-32)
Product Code:
0409-4887
Proprietary Name:
Sterile Water
Non-Proprietary Name:
Water
Substance Name:
Water
Usage Information:
DEPO-MEDROL is contraindicated in patients with known hypersensitivity to the product and its constituents. Intramuscular corticosteroid preparations are contraindicated for idiopathic thrombocytopenic purpura.DEPO-MEDROL is contraindicated for intrathecal administration. This formulation of methylprednisolone acetate has been associated with reports of severe medical events when administered by this route. DEPO-MEDROL is contraindicated in systemic fungal infections, except when administered as an intra-articular injection for localized joint conditions (see WARNINGS: Infections, Fungal Infections). Lidocaine hydrochloride is contraindicated in patients with a known history of hypersensitivity to local anesthetics of the amide type. Bupivacaine hydrochloride injection is contraindicated in obstetrical paracervical block anesthesia. Its use in this technique has resulted in fetal bradycardia and death. Bupivacaine hydrochloride injection is contraindicated in patients with a known hypersensitivity to it or to any local anesthetic agent of the amide-type. Sterile Water for Injection, USP must be made approximately isotonic prior to use.
11-Digit NDC Billing Format:
00409488734
NDC to RxNorm Crosswalk:
  • RxCUI: 1725078 - BUPivacaine HCl 0.25 % in 10 ML Injection
  • RxCUI: 1725078 - 10 ML bupivacaine hydrochloride 2.5 MG/ML Injection
  • RxCUI: 1725078 - bupivacaine HCl 0.25 % in 10 ML Injection
  • RxCUI: 1725082 - BUPivacaine HCl 0.25 % in 30 ML Injection
  • RxCUI: 1725082 - 30 ML bupivacaine hydrochloride 2.5 MG/ML Injection
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Hospira, Inc.
    Dosage Form:
    Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
    Administration Route(s):
  • 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.
    • Active Ingredient(s):
  • WATER 1 mL/mL
    • Sample Package:
    No
    FDA Application Number:
    NDA018801
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    06-16-2005
    Listing Expiration Date:
    12-31-2025
    Exclude Flag:
    N
    Code Structure:

    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 disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    0409-4887-1025 VIAL, PLASTIC in 1 TRAY / 10 mL in 1 VIAL, PLASTIC (0409-4887-17)
    0409-4887-2025 VIAL, PLASTIC in 1 TRAY / 20 mL in 1 VIAL, PLASTIC (0409-4887-23)
    0409-4887-5025 VIAL, PLASTIC in 1 TRAY / 50 mL in 1 VIAL, PLASTIC (0409-4887-24)
    0409-4887-9925 VIAL, GLASS in 1 CASE / 100 mL in 1 VIAL, GLASS (0409-4887-25)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0409-4887-34?

    The NDC Packaged Code 0409-4887-34 is assigned to a 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.. The product's dosage form is injection and is administered via intramuscular; intravenous; subcutaneous form.

    Is NDC 0409-4887 included in the NDC Directory?

    Yes, Sterile Water with product code 0409-4887 is active and included in the NDC Directory. The product was first marketed by Hospira, Inc. on June 16, 2005 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 0409-4887-34?

    The 11-digit format is 00409488734. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 4-4-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    4-4-20409-4887-345-4-200409-4887-34