NDC Package 48102-053-05 Phospholine Iodide

Echothiophate Iodide For Ophthalmic Solution Kit Ophthalmic - 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:
48102-053-05
Package Description:
1 KIT in 1 CARTON * 6.25 mL in 1 BOTTLE (48102-054-05) * 5 mL in 1 BOTTLE (48102-055-05)
Product Code:
Proprietary Name:
Phospholine Iodide
Non-Proprietary Name:
Echothiophate Iodide For Ophthalmic Solution
Usage Information:
This medication is used to treat high pressure inside the eye (due to conditions such as certain types of glaucoma) and other eye problems (such as accommodative esotropia). It works by causing the pupil to shrink, decreasing the amount of fluid within the eye, and affecting certain eye muscles.
11-Digit NDC Billing Format:
48102005305
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 205739 - Phospholine Iodide 0.125 % Ophthalmic Solution
  • RxCUI: 205739 - echothiophate iodide 1.25 MG/ML Ophthalmic Solution [Phospholine Iodide]
  • RxCUI: 205739 - Phospholine Iodide 1.25 MG/ML Ophthalmic Solution
  • RxCUI: 205739 - Phospholine Iodide 6.25 MG per 5 ML Ophthalmic Solution
  • RxCUI: 310049 - echothiophate iodide 0.125 % Ophthalmic Solution
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Fera Pharmaceuticals, Llc
    Dosage Form:
    Kit - A packaged collection of related material.
    Administration Route(s):
  • Ophthalmic - Administration to the external eye.
  • Sample Package:
    No
    FDA Application Number:
    NDA011963
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    11-17-2021
    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 48102-053-05?

    The NDC Packaged Code 48102-053-05 is assigned to a package of 1 kit in 1 carton * 6.25 ml in 1 bottle (48102-054-05) * 5 ml in 1 bottle (48102-055-05) of Phospholine Iodide, a human prescription drug labeled by Fera Pharmaceuticals, Llc. The product's dosage form is kit and is administered via ophthalmic form.

    Is NDC 48102-053 included in the NDC Directory?

    Yes, Phospholine Iodide with product code 48102-053 is active and included in the NDC Directory. The product was first marketed by Fera Pharmaceuticals, Llc on November 17, 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 48102-053-05?

    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 48102-053-05?

    The 11-digit format is 48102005305. 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
    5-3-248102-053-055-4-248102-0053-05