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  4. NDC Product Code: 66621-4000 Cystadane

NDC 66621-4000 Cystadane

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 66621-4000?
  5. Cystadane Uses
  6. Active Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
66621-4000
Proprietary Name:
Cystadane
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rare Disease Therapeutics, Inc.
Labeler Code:
66621
Product Label ID:
84f7c21f-d0af-4ae6-9cd5-d5af96ade329
Start Marketing Date: [9]
10-25-1996
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - NONE)

Product Packages

NDC Code 66621-4000-1

Package Description: 180 POWDER, FOR SOLUTION in 1 BOTTLE

Product Details

What is NDC 66621-4000?

The NDC code 66621-4000 is assigned by the FDA to the product Cystadane which is product labeled by Rare Disease Therapeutics, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 66621-4000-1 180 powder, for solution in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Cystadane?

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.

Which are Cystadane UNII Codes?

The UNII codes for the active ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Cystadane?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 404539 - Cystadane 1 GM/Scoop Powder for Oral Solution
  • RxCUI: 404539 - betaine 1000 MG Powder for Oral Solution [Cystadane]
  • RxCUI: 404539 - Cystadane 1000 MG (as betaine anhydrous) Powder for Oral Solution
  • RxCUI: 404539 - Cystadane 1000 MG Powder for Oral Solution
  • RxCUI: 562847 - betaine anhydrous 1 GM/Scoop Powder for Oral Solution

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".