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  4. NDC Product Code: 49643-705 Standardized Cat Hair

NDC 49643-705 Standardized Cat Hair

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 49643-705?
  4. Standardized Cat Hair Uses
  5. Active Ingredients UNII Codes
  6. Inactive 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:
49643-705
Proprietary Name:
Standardized Cat Hair
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Allermed Laboratories, Inc.
Labeler Code:
49643
Product Label ID:
abffdafd-f922-44ab-8e98-972a72ca1004
Start Marketing Date: [9]
08-15-1992
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 49643-705-05

Package Description: 5 mL in 1 VIAL, MULTI-DOSE

NDC Code 49643-705-10

Package Description: 10 mL in 1 VIAL, MULTI-DOSE

NDC Code 49643-705-30

Package Description: 30 mL in 1 VIAL, MULTI-DOSE

NDC Code 49643-705-50

Package Description: 50 mL in 1 VIAL, MULTI-DOSE

Product Details

What is NDC 49643-705?

The NDC code 49643-705 is assigned by the FDA to the product Standardized Cat Hair which is product labeled by Allermed Laboratories, Inc.. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 49643-705-05 5 ml in 1 vial, multi-dose , 49643-705-10 10 ml in 1 vial, multi-dose , 49643-705-30 30 ml in 1 vial, multi-dose , 49643-705-50 50 ml in 1 vial, multi-dose . 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 Standardized Cat Hair?

Studies have shown that skin tests with cat extract are useful in the diagnosis of cat allergy. As a rule, persons with cat allergy have positive skin reactions when tested with cat extract, and non-allergic individuals rarely react7, 8, 9. However, the relationship between a positive skin test and the appearance of clinical symptoms after exposure to a cat is not absolute, i.e., some skin-test positive persons do not experience allergic symptoms after exposure10. Failure to experience symptoms may be dose related, since it is known that cats vary significantly in the amount of Fel d1 they produce11. The efficacy of cat extract immunotherapy in the treatment of bronchial asthma has been shown in two studies12, 13. A reduction in bronchial sensitivity was observed in five patients with cat allergy, whereas no reduction was observed in placebo treated, cat-allergic patients.

Which are Standardized Cat Hair UNII Codes?

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

Which are Standardized Cat Hair 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:

What is the NDC to RxNorm Crosswalk for Standardized Cat Hair?

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: 851948 - cat hair extract 10,000 BAU/mL Injectable Solution
  • RxCUI: 851948 - cat hair extract 10000 BAU/ML Injectable Solution
  • RxCUI: 851948 - Felis catus hair extract 10,000 BAU/ML Injectable 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".