NDC Package 72647-900-01 Betaine Anhydrous For Oral Solution

Betaine Anhydrous For Solution 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:
72647-900-01
Package Description:
180 g in 1 BOTTLE
Product Code:
Proprietary Name:
Betaine Anhydrous For Oral Solution
Non-Proprietary Name:
Betaine Anhydrous
Substance Name:
Betaine
Usage Information:
This medication is used to treat high levels of a certain important body chemical (homocysteine) due to an inherited disorder (homocystinuria). Decreasing high homocysteine levels may help prevent serious blood clots, abnormal bone formation, brittle bones (osteoporosis), and eye problems (e.g., dislocated eye lens, nearsightedness). This medication works by decreasing blood levels of homocysteine. It does not correct the inherited disorder that causes the disease.
11-Digit NDC Billing Format:
72647090001
Billing Unit:
GM - Billing unit of "gram" is used when a product is measured by its weight.
NDC to RxNorm Crosswalk:
180 GM
NDC to RxNorm Crosswalk:
  • RxCUI: 562847 - betaine anhydrous 1 GM/Scoop Powder for Oral Solution
  • RxCUI: 562847 - betaine 1000 MG Powder for Oral Solution
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Oakrum Pharma, Llc
    Dosage Form:
    For Solution - A product, usually a solid, intended for solution prior to administration.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA214864
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    02-03-2022
    End Marketing Date:
    04-30-2024
    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 72647-900-01?

    The NDC Packaged Code 72647-900-01 is assigned to a package of 180 g in 1 bottle of Betaine Anhydrous For Oral Solution, a human prescription drug labeled by Oakrum Pharma, Llc. The product's dosage form is for solution and is administered via oral form.This product is billed per "GM" gram and contains an estimated amount of 180 billable units per package.

    Is NDC 72647-900 included in the NDC Directory?

    Yes, Betaine Anhydrous For Oral Solution with product code 72647-900 is active and included in the NDC Directory. The product was first marketed by Oakrum Pharma, Llc on February 03, 2022.

    What is the NDC billing unit for package 72647-900-01?

    The contents of this package are billed per "gm or gram", products billed per gram are products measured by weight. The calculated billable units for this package is 180.

    What is the 11-digit format for NDC 72647-900-01?

    The 11-digit format is 72647090001. 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
    5-3-272647-900-015-4-272647-0900-01