NDC Package 73684-150-60 Cataflam

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
73684-150-60
Package Description:
60 TABLET in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Cataflam
Usage Information:
Carefully consider the potential benefits and risks of diclofenac potassium tablets and other treatment options before deciding to use diclofenac potassium tablets. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see WARNINGS, Gastrointestinal Bleeding, Ulceration, and Perforation).Diclofenac potassium tablets are indicated:For treatment of primary dysmenorrheaFor relief of mild to moderate painFor relief of the signs and symptoms of osteoarthritisFor relief of the signs and symptoms of rheumatoid arthritis
11-Digit NDC Billing Format:
73684015060
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
60 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 855942 - diclofenac potassium 50 MG Oral Tablet
  • RxCUI: 855942 - Diclofenac K+ 50 MG Oral Tablet
  • RxCUI: 855942 - Diclofenac Pot 50 MG Oral Tablet
  • RxCUI: 855944 - Cataflam 50 MG Oral Tablet
  • RxCUI: 855944 - diclofenac potassium 50 MG Oral Tablet [Cataflam]
  • Labeler Name:
    Blucrest Pharmaceuticals, Llc
    Sample Package:
    No
    Start Marketing Date:
    12-14-2020
    Listing Expiration Date:
    12-31-2022
    Exclude Flag:
    I
    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 73684-150-60?

    The NDC Packaged Code 73684-150-60 is assigned to a package of 60 tablet in 1 bottle, plastic of Cataflam, labeled by Blucrest Pharmaceuticals, Llc. The product's dosage form is and is administered via form.This product is billed for "EA" each discreet unit and contains an estimated amount of 60 billable units per package.

    Is NDC 73684-150 included in the NDC Directory?

    No, Cataflam with product code 73684-150 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Blucrest Pharmaceuticals, Llc on December 14, 2020 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 73684-150-60?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 60.

    What is the 11-digit format for NDC 73684-150-60?

    The 11-digit format is 73684015060. 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
    5-3-273684-150-605-4-273684-0150-60