NDC Package 0338-9591-12 Plasma-lyte A

Sodium Chloride,Sodium Gluconate,Sodium Acetate,Potassium Chloride And Magnesium Chloride - 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:
0338-9591-12
Package Description:
12 BAG in 1 CARTON / 1000 mL in 1 BAG (0338-9591-01)
Product Code:
Proprietary Name:
Plasma-lyte A
Non-Proprietary Name:
Sodium Chloride, Sodium Gluconate, Sodium Acetate, Potassium Chloride And Magnesium Chloride
Substance Name:
Magnesium Chloride; Potassium Chloride; Sodium Acetate; Sodium Chloride; Sodium Gluconate
11-Digit NDC Billing Format:
00338959112
NDC to RxNorm Crosswalk:
  • RxCUI: 801109 - magnesium chloride 0.00148 MEQ/mL / potassium chloride 0.00497 MEQ/mL / sodium acetate 0.027 MEQ/mL / sodium chloride 0.0899 MEQ/mL / sodium gluconate 5.02 MG/mL Injectable Solution
  • RxCUI: 801109 - magnesium chloride 0.00148 MEQ/ML / potassium chloride 0.00497 MEQ/ML / sodium acetate 0.027 MEQ/ML / sodium chloride 0.0899 MEQ/ML / sodium gluconate 5.02 MG/ML Injectable Solution
  • RxCUI: 801109 - Magnesium Chloride 0.00148 MEQ/ML / K+ Chloride 0.00497 MEQ/ML / Sodium Acetate 0.027 MEQ/ML / NaCl 0.0899 MEQ/ML / Sodium gluconate 5.02 MG/ML Injectable Solution
  • RxCUI: 801109 - Magnesium Chloride 0.00148 MEQ/ML / Pot Chloride 0.00497 MEQ/ML / Sodium Acetate 0.027 MEQ/ML / NaCl 0.0899 MEQ/ML / Sodium gluconate 5.02 MG/ML Injectable Solution
  • RxCUI: 801112 - Plasma-Lyte A pH 7.4 Injectable Solution
Product Type:
Human Prescription Drug
Labeler Name:
Baxter Healthcare Company
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):
Intravenous - Administration within or into a vein or veins.
Sample Package:
No
Marketing Category:
UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE -
Start Marketing Date:
11-06-2024
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 0338-9591-12?

The NDC Packaged Code 0338-9591-12 is assigned to a package of 12 bag in 1 carton / 1000 ml in 1 bag (0338-9591-01) of Plasma-lyte A, a human prescription drug labeled by Baxter Healthcare Company. The product's dosage form is injection, solution and is administered via intravenous form.

Is NDC 0338-9591 included in the NDC Directory?

Yes, Plasma-lyte A with product code 0338-9591 is active and included in the NDC Directory. The product was first marketed by Baxter Healthcare Company on November 06, 2024 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 0338-9591-12?

The 11-digit format is 00338959112. 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
4-4-20338-9591-125-4-200338-9591-12