NDC Package 70512-865-15 Phenylephrine Hydrochloride

Solution/ Drops 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:
70512-865-15
Package Description:
1 BOTTLE, DROPPER in 1 CARTON / 15 mL in 1 BOTTLE, DROPPER
Product Code:
Proprietary Name:
Phenylephrine Hydrochloride
Non-Proprietary Name:
Phenylephrine Hydrochloride
Substance Name:
Phenylephrine Hydrochloride
Usage Information:
Phenylephrine Hydrochloride Ophthalmic Solution, USP 2.5% and 10%, is indicated to dilate the pupil.
11-Digit NDC Billing Format:
70512086515
NDC to RxNorm Crosswalk:
  • RxCUI: 1234571 - phenylephrine HCl 10 % Ophthalmic Solution
  • RxCUI: 1234571 - phenylephrine hydrochloride 100 MG/ML Ophthalmic Solution
  • RxCUI: 1234571 - phenylephrine hydrochloride 10 % Ophthalmic Solution
  • RxCUI: 1234579 - phenylephrine HCl 2.5 % Ophthalmic Solution
  • RxCUI: 1234579 - phenylephrine hydrochloride 25 MG/ML Ophthalmic Solution
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Sola Pharmaceuticals, Llc
    Dosage Form:
    Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
    Administration Route(s):
  • Ophthalmic - Administration to the external eye.
  • Sample Package:
    No
    FDA Application Number:
    ANDA215183
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    06-01-2024
    Listing Expiration Date:
    12-31-2025
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    70512-865-021 BOTTLE, DROPPER in 1 CARTON / 2 mL in 1 BOTTLE, DROPPER

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 70512-865-15?

    The NDC Packaged Code 70512-865-15 is assigned to a package of 1 bottle, dropper in 1 carton / 15 ml in 1 bottle, dropper of Phenylephrine Hydrochloride, a human prescription drug labeled by Sola Pharmaceuticals, Llc. The product's dosage form is solution/ drops and is administered via ophthalmic form.

    Is NDC 70512-865 included in the NDC Directory?

    Yes, Phenylephrine Hydrochloride with product code 70512-865 is active and included in the NDC Directory. The product was first marketed by Sola Pharmaceuticals, Llc on June 01, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 70512-865-15?

    The 11-digit format is 70512086515. 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
    5-3-270512-865-155-4-270512-0865-15