NDC Package 84549-966-07 Bacteriostatic Sodium Chloride

Sodium Chloride Injection, Solution Intramuscular; Intravenous; Subcutaneous - View Billable Units, 11-Digit Format, RxNorm

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:
84549-966-07
Package Description:
30 mL in 1 VIAL, MULTI-DOSE
Product Code:
Proprietary Name:
Bacteriostatic Sodium Chloride
Non-Proprietary Name:
Sodium Chloride
Substance Name:
Sodium Chloride
Usage Information:
This product is used to treat dryness inside the nose (nasal passages). It helps add moisture inside the nose to dissolve and soften thick or crusty mucus. In babies and young children with stuffy noses who cannot blow their noses, using this product helps to make the mucus easier to remove with a nasal bulb syringe. This helps relieve stuffiness and makes breathing easier. This product contains a purified gentle salt solution (also called saline or sodium chloride solution). It does not contain any medication.
11-Digit NDC Billing Format:
84549096607
Product Type:
Human Prescription Drug
Labeler Name:
Propharma Distribution
Dosage Form:
Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.
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):
Sample Package:
No
FDA Application Number:
NDA018800
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
04-30-2005
Listing Expiration Date:
12-31-2026
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.

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Frequently Asked Questions

What is NDC 84549-966-07?

The NDC Packaged Code 84549-966-07 is assigned to a package of 30 ml in 1 vial, multi-dose of Bacteriostatic Sodium Chloride, a human prescription drug labeled by Propharma Distribution. The product's dosage form is injection, solution and is administered via intramuscular; intravenous; subcutaneous form.

Is NDC 84549-966 included in the NDC Directory?

Yes, Bacteriostatic Sodium Chloride with product code 84549-966 is active and included in the NDC Directory. The product was first marketed by Propharma Distribution on April 30, 2005 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 84549-966-07?

The 11-digit format is 84549096607. 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 5-3-2 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
5-3-284549-966-075-4-284549-0966-07