NDC Package 55315-844-20 Naproxen Sodium Pm

Naproxen Sodium Tablet 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:
55315-844-20
Package Description:
1 BOTTLE, PLASTIC in 1 BOX / 20 TABLET in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Naproxen Sodium Pm
Non-Proprietary Name:
Naproxen Sodium
Substance Name:
Diphenhydramine Hydrochloride; Naproxen Sodium
Usage Information:
Naproxen is used to relieve pain from various conditions. It also reduces pain, swelling, and joint stiffness caused by arthritis, bursitis, and gout attacks. This medication is known as a nonsteroidal anti-inflammatory drug (NSAID). It works by blocking your body's production of certain natural substances that cause inflammation. If you are treating a chronic condition such as arthritis, ask your doctor about non-drug treatments and/or using other medications to treat your pain. See also Warning section. Some brands of sustained-release naproxen take longer to be absorbed and are not recommended for pain that needs quick relief (such as during a gout attack). Ask your doctor or pharmacist if you have questions about your particular brand.
11-Digit NDC Billing Format:
55315084420
NDC to RxNorm Crosswalk:
  • RxCUI: 1550957 - diphenhydrAMINE HCl 25 MG / naproxen sodium 220 MG Oral Tablet
  • RxCUI: 1550957 - diphenhydramine hydrochloride 25 MG / naproxen sodium 220 MG Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Freds Inc
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    ANDA209726
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    02-28-2019
    End Marketing Date:
    06-30-2024
    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 55315-844-20?

    The NDC Packaged Code 55315-844-20 is assigned to a package of 1 bottle, plastic in 1 box / 20 tablet in 1 bottle, plastic of Naproxen Sodium Pm, a human over the counter drug labeled by Freds Inc. The product's dosage form is tablet and is administered via oral form.

    Is NDC 55315-844 included in the NDC Directory?

    Yes, Naproxen Sodium Pm with product code 55315-844 is active and included in the NDC Directory. The product was first marketed by Freds Inc on February 28, 2019.

    What is the 11-digit format for NDC 55315-844-20?

    The 11-digit format is 55315084420. 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
    5-3-255315-844-205-4-255315-0844-20