NDC Package 69238-2026-7 Amlodipine

Suspension Oral - 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:
69238-2026-7
Package Description:
1 BOTTLE in 1 CARTON / 150 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Amlodipine
Non-Proprietary Name:
Amlodipine
Substance Name:
Amlodipine Benzoate
Usage Information:
Amlodipine is used with or without other medications to treat high blood pressure. Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems. Amlodipine belongs to a class of drugs known as calcium channel blockers. It works by relaxing blood vessels so blood can flow more easily. Amlodipine is also used to prevent certain types of chest pain (angina). It may help to increase your ability to exercise and decrease the frequency of angina attacks. It should not be used to treat attacks of chest pain when they occur. Use other medications (such as sublingual nitroglycerin) to relieve attacks of chest pain as directed by your doctor.
11-Digit NDC Billing Format:
69238202607
NDC to RxNorm Crosswalk:
  • RxCUI: 2184120 - amLODIPine 1 MG/mL Oral Suspension
  • RxCUI: 2184120 - amlodipine 1 MG/ML Oral Suspension
  • RxCUI: 2184120 - amlodipine 1 MG/ML (as amlodipine benzoate 1.3 MG/ML) Oral Suspension
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Amneal Pharmaceuticals Ny Llc
    Dosage Form:
    Suspension - A liquid1 dosage form that contains solid particles dispersed in a liquid vehicle.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA215035
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    06-16-2023
    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.

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    Frequently Asked Questions

    What is NDC 69238-2026-7?

    The NDC Packaged Code 69238-2026-7 is assigned to a package of 1 bottle in 1 carton / 150 ml in 1 bottle of Amlodipine, a human prescription drug labeled by Amneal Pharmaceuticals Ny Llc. The product's dosage form is suspension and is administered via oral form.

    Is NDC 69238-2026 included in the NDC Directory?

    Yes, Amlodipine with product code 69238-2026 is active and included in the NDC Directory. The product was first marketed by Amneal Pharmaceuticals Ny Llc on June 16, 2023 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 11-digit format for NDC 69238-2026-7?

    The 11-digit format is 69238202607. 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 5-4-1 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
    5-4-169238-2026-75-4-269238-2026-07