NDC Package 72988-0011-1 Baenosin

Platycodon Root,Licorice,Jujube,Peony Root Capsule 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:
72988-0011-1
Package Description:
10 CAPSULE in 1 PACKAGE
Product Code:
Proprietary Name:
Baenosin
Non-Proprietary Name:
Platycodon Root, Licorice, Jujube, Peony Root
Substance Name:
Ginger; Jujube Fruit; Licorice; Paeonia Lactiflora Root; Platycodon Grandiflorum Root; Poncirus Trifoliata Fruit
Usage Information:
Adults take 2 capsules 3 times a day before meals or between meals
11-Digit NDC Billing Format:
72988001101
Product Type:
Human Otc Drug
Labeler Name:
Lydia Co., Ltd.
Dosage Form:
Capsule - A solid oral dosage form consisting of a shell and a filling. The shell is composed of a single sealed enclosure, or two halves that fit together and which are sometimes sealed with a band. Capsule shells may be made from gelatin, starch, or cellulose, or other suitable materials, may be soft or hard, and are filled with solid or liquid ingredients that can be poured or squeezed.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    Marketing Category:
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date:
    04-22-2019
    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.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 72988-0011-1?

    The NDC Packaged Code 72988-0011-1 is assigned to a package of 10 capsule in 1 package of Baenosin, a human over the counter drug labeled by Lydia Co., Ltd.. The product's dosage form is capsule and is administered via oral form.

    Is NDC 72988-0011 included in the NDC Directory?

    Yes, Baenosin with product code 72988-0011 is active and included in the NDC Directory. The product was first marketed by Lydia Co., Ltd. on April 22, 2019 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 72988-0011-1?

    The 11-digit format is 72988001101. 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
    5-4-172988-0011-15-4-272988-0011-01