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  4. NDC Product Code: 49643-702 House Dust Mite, Dermatophagoides Farinae

NDC 49643-702 House Dust Mite, Dermatophagoides Farinae

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 49643-702?
  4. House Dust Mite, Dermatophagoides Farinae 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:
49643-702
Proprietary Name:
House Dust Mite, Dermatophagoides Farinae
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Allermed Laboratories, Inc.
Labeler Code:
49643
Product Label ID:
3b19e1e4-1a28-4515-ac20-cc4a9b2d45e6
Start Marketing Date: [9]
12-24-1986
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 49643-702-05

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

NDC Code 49643-702-10

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

NDC Code 49643-702-30

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

NDC Code 49643-702-50

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

Product Details

What is NDC 49643-702?

The NDC code 49643-702 is assigned by the FDA to the product House Dust Mite, Dermatophagoides Farinae 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 49643-702-05 5 ml in 1 vial, multi-dose , 49643-702-10 10 ml in 1 vial, multi-dose , 49643-702-30 30 ml in 1 vial, multi-dose , 49643-702-50 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 House Dust Mite, Dermatophagoides Farinae?

Standardized mite extract is indicated for use in the diagnosis of patients with a history of allergy to mites or house dust and for the treatment of patients with a history of mite allergy who have established sensitivity to mites by diagnostic skin testing. The use of mite extract for the above purposes should be made only by physicians with special familiarity and knowledge of allergy as described in a standard allergy textbook 10.

Which are House Dust Mite, Dermatophagoides Farinae UNII Codes?

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

  • DERMATOPHAGOIDES FARINAE (UNII: PR9U2YPF3Q)
  • DERMATOPHAGOIDES FARINAE (UNII: PR9U2YPF3Q) (Active Moiety)

Which are House Dust Mite, Dermatophagoides Farinae 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 House Dust Mite, Dermatophagoides Farinae?

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: 852825 - American house dust mite extract 10000 AU/ML Injectable Solution
  • RxCUI: 852825 - American house dust mite allergenic extract 10000 AU/ML Injectable Solution
  • RxCUI: 852825 - Dermatophagoides farinae extract 10,000 AU/ML Injectable Solution
  • RxCUI: 852829 - European house dust mite extract 10000 AU/ML Injectable Solution
  • RxCUI: 852829 - European house dust mite allergenic extract 10000 AU/ML Injectable Solution

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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".