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  4. NDC Product Code: 44738-8001 Ginsamin Power

NDC 44738-8001 Ginsamin Power

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 44738-8001?
  5. Active Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
44738-8001
Proprietary Name:
Ginsamin Power
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Biogrand Co., Ltd
Labeler Code:
44738
Product Label ID:
79fdfc31-a9fb-4b79-95d9-a792f982bd14
Start Marketing Date: [9]
03-07-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
RED (C48326 - DARK RED)
Shape:
OVAL (C48345)
Size(s):
15 MM
Imprint(s):
3;HP;X
Score:
1

Product Packages

NDC Code 44738-8001-1

Package Description: 60 TABLET in 1 BOX

Product Details

What is NDC 44738-8001?

The NDC code 44738-8001 is assigned by the FDA to the product Ginsamin Power which is product labeled by Biogrand Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 44738-8001-1 60 tablet in 1 box . 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.

Which are Ginsamin Power UNII Codes?

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

* 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".