NDC Package 17856-0162-3 Phenobarbital With Belladonna Alkaloids

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:
17856-0162-3
Package Description:
5 mL in 1 CUP, UNIT-DOSE
Product Code:
Proprietary Name:
Phenobarbital With Belladonna Alkaloids
Usage Information:
Possibly effective for use as adjunctive therapy in the treatment of irritable bowel syndrome (irritable colon, spastic colon, mucous colitis) and acute enterocolitis. May also be useful as adjunctive therapy in the treatment of duodenal ulcer.IT HAS NOT BEEN SHOWN CONCLUSIVELY WHETHER ANTICHOLINERGIC/ANTISPASMODIC DRUGS AID IN THE HEALING OF A DUODENAL ULCER, DECREASE THE RATE OF RECURRENCES OR PREVENT COMPLICATIONS.
11-Digit NDC Billing Format:
17856016203
NDC to RxNorm Crosswalk:
  • RxCUI: 1046787 - PHENobarbital 16.2 MG / hyoscyamine sulfate 0.1037 MG / atropine sulfate 0.0194 MG / scopolamine HBr 0.0065 MG in 5 mL Oral Solution
  • RxCUI: 1046787 - atropine sulfate 0.00388 MG/ML / hyoscyamine sulfate 0.0207 MG/ML / phenobarbital 3.24 MG/ML / scopolamine hydrobromide 0.0013 MG/ML Oral Solution
  • RxCUI: 1046787 - atropine sulfate 0.0194 MG / hyoscyamine sulfate 0.1037 MG / phenobarbital 16.2 MG / scopolamine hydrobromide 0.0065 MG per 5 ML Oral Solution
  • Labeler Name:
    Atlantic Biologicals Corp.
    Sample Package:
    No
    Start Marketing Date:
    05-21-2018
    Listing Expiration Date:
    12-31-2019
    Exclude Flag:
    I

    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
    17856-0162-110 mL in 1 CUP, UNIT-DOSE
    17856-0162-25 mL in 1 CUP, UNIT-DOSE
    17856-0162-410 CUP, UNIT-DOSE in 1 BOX / 10 mL in 1 CUP, UNIT-DOSE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 17856-0162-3?

    The NDC Packaged Code 17856-0162-3 is assigned to a package of 5 ml in 1 cup, unit-dose of Phenobarbital With Belladonna Alkaloids, labeled by Atlantic Biologicals Corp.. The product's dosage form is and is administered via form.

    Is NDC 17856-0162 included in the NDC Directory?

    No, Phenobarbital With Belladonna Alkaloids with product code 17856-0162 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Atlantic Biologicals Corp. on May 21, 2018 and its listing in the NDC Directory is set to expire on December 31, 2019 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 17856-0162-3?

    The 11-digit format is 17856016203. 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
    5-4-117856-0162-35-4-217856-0162-03