Phenylephrine Hydrochloride Injection, Solution
NDC Package 43598-182-05

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Phenylephrine Hydrochloride Injection, Solution injection is phenylephrine Hydrochloride in 0.9% Sodium Chloride Injection is indicated for increasing blood pressure in adults with clinically important hypotension resulting primarily from vasodilation in the setting of anesthesia. This formulation utilizes a injection, solution delivery system. Marketed by Dr. Reddy's Laboratories Inc., this product is identified by NDC 43598-182 and is authorized under FDA application NDA216830.

Identification & Billing

NDC Package Code
43598-182-05
Package Description
5 BAG in 1 CARTON / 250 mL in 1 BAG (43598-182-50)
Product Code
43598-182
11-Digit Billing Format
43598018205
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
RxNorm Crosswalk
  • RxCUI: 2717659 - phenylephrine hydrochloride 20 MG in 250 ML Injection
  • RxCUI: 2717659 - 250 ML phenylephrine hydrochloride 0.08 MG/ML Injection
  • RxCUI: 2717659 - phenylephrine hydrochloride 0.08 MG/ML per 250 ML Injection
  • RxCUI: 2717659 - phenylephrine hydrochloride 20 MG (phenylephrine 16.4 MG) per 250 ML Injection
  • RxCUI: 2717659 - phenylephrine hydrochloride 20 MG per 250 ML Injection

Clinical Specifications

Proprietary Name
Phenylephrine Hydrochloride Injection, Solution
Non-Proprietary Name
Phenylephrine Hydrochloride Injection, Solution
Substance Name
Phenylephrine
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
Intravenous - Administration within or into a vein or veins.
Active Ingredient(s)
PHENYLEPHRINE 80 ug/mL
Pharmacologic Class
Usage Information
Phenylephrine Hydrochloride in 0.9% Sodium Chloride Injection is indicated for increasing blood pressure in adults with clinically important hypotension resulting primarily from vasodilation in the setting of anesthesia.

Regulatory & Marketing

Labeler Name
Dr. Reddy's Laboratories Inc.
Product Type
Human Prescription Drug
FDA Application #
NDA216830
Marketing Category
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date
07-01-2025
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 43598-182-05 identifies a specific commercial package of 5 bag in 1 carton / 250 ml in 1 bag (43598-182-50) of Phenylephrine Hydrochloride Injection, Solution, a human prescription drug labeled by Dr. Reddy's Laboratories Inc.. This injection, solution is formulated for intravenous use and contains phenylephrine 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 Dr. Reddy's Laboratories Inc. on July 01, 2025. The current certification is valid through December 31, 2027.

How is this Dr. Reddy's Laboratories Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 43598018205. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. 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:

10-Digit Format (5-3-2)
43598-182-05
11-Digit CMS (5-4-2)
43598-0182-05

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.