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  4. NDC Product Code: 53346-1347 Dr. Reckeweg R47 Neuroglobin Combination Product

NDC 53346-1347 Dr. Reckeweg R47 Neuroglobin Combination Product

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 53346-1347?
  4. Dr. Reckeweg R47 Neuroglobin Combination Product Uses
  5. Active Ingredients UNII Codes
  6. Inactive 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:
53346-1347
Proprietary Name:
Dr. Reckeweg R47 Neuroglobin Combination Product
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Pharmazeutische Fabrik Dr. Reckeweg & Co
Labeler Code:
53346
Product Label ID:
d6d6e365-6278-49d0-8696-8dd8a22da818
Start Marketing Date: [9]
06-01-1986
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 53346-1347-5

Package Description: 50 mL in 1 BOTTLE

Product Details

What is NDC 53346-1347?

The NDC code 53346-1347 is assigned by the FDA to the product Dr. Reckeweg R47 Neuroglobin Combination Product which is product labeled by Pharmazeutische Fabrik Dr. Reckeweg & Co. The product's dosage form is . The product is distributed in a single package with assigned NDC code 53346-1347-5 50 ml 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 Dr. Reckeweg R47 Neuroglobin Combination Product?

UsesFor the temporary relief of:Nervous exhaustionAnguish and anxietyDiscomfort associated with PMS

Which are Dr. Reckeweg R47 Neuroglobin Combination Product UNII Codes?

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

Which are Dr. Reckeweg R47 Neuroglobin Combination Product Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

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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".