NDC Package 71863-202-06 Biorphen

Phenylephrine Hydrochloride Injection, Solution 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:
71863-202-06
Package Description:
10 AMPULE in 1 CARTON / 5 mL in 1 AMPULE (71863-202-05)
Product Code:
Proprietary Name:
Biorphen
Non-Proprietary Name:
Phenylephrine Hydrochloride
Substance Name:
Phenylephrine Hydrochloride
Usage Information:
BIORPHEN is indicated for the treatment of clinically important hypotension resulting primarily from vasodilation in the setting of anesthesia.
11-Digit NDC Billing Format:
71863020206
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1666372 - phenylephrine HCl 10 MG in 1 ML Injection
  • RxCUI: 1666372 - 1 ML phenylephrine hydrochloride 10 MG/ML Injection
  • RxCUI: 1666372 - phenylephrine HCl 10 MG per 1 ML Injection
  • RxCUI: 2262018 - phenylephrine hydrochloride 500 MCG in 5 mL Injection
  • RxCUI: 2262018 - 5 ML phenylephrine hydrochloride 0.1 MG/ML Injection
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Eton Pharmaceuticals, Inc.
    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
    FDA Application Number:
    NDA212909
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    11-15-2019
    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 71863-202-06?

    The NDC Packaged Code 71863-202-06 is assigned to a package of 10 ampule in 1 carton / 5 ml in 1 ampule (71863-202-05) of Biorphen, a human prescription drug labeled by Eton Pharmaceuticals, Inc.. The product's dosage form is injection, solution and is administered via intravenous form.

    Is NDC 71863-202 included in the NDC Directory?

    Yes, Biorphen with product code 71863-202 is active and included in the NDC Directory. The product was first marketed by Eton Pharmaceuticals, Inc. on November 15, 2019 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 71863-202-06?

    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 71863-202-06?

    The 11-digit format is 71863020206. 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
    5-3-271863-202-065-4-271863-0202-06