NDC Package 68308-220-01 Esgic

Butalbital,Acetaminophen And Caffeine 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:
68308-220-01
Package Description:
100 TABLET in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Esgic
Non-Proprietary Name:
Butalbital, Acetaminophen And Caffeine
Substance Name:
Acetaminophen; Butalbital; Caffeine
Usage Information:
This combination medication is used to treat tension headaches. Acetaminophen helps to decrease the pain from the headache. Caffeine helps increase the effects of acetaminophen. Butalbital is a sedative that helps to decrease anxiety and cause sleepiness and relaxation.
11-Digit NDC Billing Format:
68308022001
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
100 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 211189 - ESGIC 50 MG / 325 MG / 40 MG Oral Tablet
  • RxCUI: 211189 - acetaminophen 325 MG / butalbital 50 MG / caffeine 40 MG Oral Tablet [Esgic]
  • RxCUI: 211189 - APAP 325 MG / butalbital 50 MG / Caffeine 40 MG Oral Tablet [Esgic]
  • RxCUI: 211189 - Esgic (APAP 325 MG / butalbital 50 MG / caffeine 40 MG) Oral Tablet
  • RxCUI: 238154 - butalbital 50 MG / acetaminophen 325 MG / caffeine 40 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Mayne Pharma 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.
  • DEA Schedule:
    Schedule III (CIII) Substances
    Sample Package:
    No
    FDA Application Number:
    ANDA089175
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    05-01-2014
    End Marketing Date:
    03-31-2025
    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.

    Frequently Asked Questions

    What is NDC 68308-220-01?

    The NDC Packaged Code 68308-220-01 is assigned to a package of 100 tablet in 1 bottle, plastic of Esgic, a human prescription drug labeled by Mayne Pharma Inc.. The product's dosage form is tablet and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 100 billable units per package.

    Is NDC 68308-220 included in the NDC Directory?

    Yes, Esgic with product code 68308-220 is active and included in the NDC Directory. The product was first marketed by Mayne Pharma Inc. on May 01, 2014.

    What is the NDC billing unit for package 68308-220-01?

    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 100.

    What is the 11-digit format for NDC 68308-220-01?

    The 11-digit format is 68308022001. 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
    5-3-268308-220-015-4-268308-0220-01