NDC Package 70069-802-10 Phenylephrine Hydrochloride

Injection Intravenous - 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:
70069-802-10
Package Description:
10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON / 5 mL in 1 VIAL, PHARMACY BULK PACKAGE (70069-802-01)
Product Code:
Proprietary Name:
Phenylephrine Hydrochloride
Non-Proprietary Name:
Phenylephrine Hydrochloride
Substance Name:
Phenylephrine Hydrochloride
Usage Information:
Phenylephrine hydrochloride Injection is indicated for the treatment of clinically important hypotension resulting primarily from vasodilation in the setting of anesthesia.
11-Digit NDC Billing Format:
70069080210
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1232651 - phenylephrine HCl 10 MG/ML Injectable Solution
  • RxCUI: 1232651 - phenylephrine hydrochloride 10 MG/ML Injectable Solution
  • RxCUI: 1232651 - phenylephrine hydrochloride 1 % Injectable Solution
  • RxCUI: 1232651 - phenylephrine hydrochloride 100 MG per 10 ML Injectable Solution
  • RxCUI: 1232651 - phenylephrine hydrochloride 50 MG per 5 ML Injectable Solution
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Somerset Therapeutics, Llc
    Dosage Form:
    Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
  • Sample Package:
    No
    FDA Application Number:
    ANDA213318
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    09-22-2021
    Listing Expiration Date:
    12-31-2024
    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.

    Frequently Asked Questions

    What is NDC 70069-802-10?

    The NDC Packaged Code 70069-802-10 is assigned to a package of 10 vial, pharmacy bulk package in 1 carton / 5 ml in 1 vial, pharmacy bulk package (70069-802-01) of Phenylephrine Hydrochloride, a human prescription drug labeled by Somerset Therapeutics, Llc. The product's dosage form is injection and is administered via intravenous form.

    Is NDC 70069-802 included in the NDC Directory?

    Yes, Phenylephrine Hydrochloride with product code 70069-802 is active and included in the NDC Directory. The product was first marketed by Somerset Therapeutics, Llc on September 22, 2021 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 70069-802-10?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 70069-802-10?

    The 11-digit format is 70069080210. 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
    5-3-270069-802-105-4-270069-0802-10