NDC 49288-0280 Johnson Grass Smut

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
49288-0280
Proprietary Name:
Johnson Grass Smut
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Antigen Laboratories, Inc.
Labeler Code:
49288
Start Marketing Date: [9]
03-23-1974
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 49288-0280-1

Package Description: 2 mL in 1 VIAL, MULTI-DOSE

NDC Code 49288-0280-2

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

NDC Code 49288-0280-3

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

NDC Code 49288-0280-4

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

NDC Code 49288-0280-5

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

Product Details

What is NDC 49288-0280?

The NDC code 49288-0280 is assigned by the FDA to the product Johnson Grass Smut which is product labeled by Antigen Laboratories, Inc.. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 49288-0280-1 2 ml in 1 vial, multi-dose , 49288-0280-2 5 ml in 1 vial, multi-dose , 49288-0280-3 10 ml in 1 vial, multi-dose , 49288-0280-4 30 ml in 1 vial, multi-dose , 49288-0280-5 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 Johnson Grass Smut?

Allergenic extract is used for diagnostic testing and for the treatment (immunotherapy) of patients whose histories indicate that upon natural exposure to the allergen, they experience allergic symptoms. Confirmation is determined by skin testing. Diagnostic use of allergenic extracts usually begins with direct skin testing. This product is not intended for treatment of patients who do not manifest immediate hypersensitivity reactions to the allergenic extract following skin testing.

Which are Johnson Grass Smut UNII Codes?

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

Which are Johnson Grass Smut 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 Johnson Grass Smut?

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: 1006282 - Apiospora montagnei allergenic extract 50 MG/ML Injectable Solution
  • RxCUI: 1006282 - Apiospora montagnei allergenic extract 0.05 GM/ML Injectable Solution
  • RxCUI: 1006288 - Aspergillus flavus allergenic extract 50 MG/ML Injectable Solution
  • RxCUI: 1006288 - Aspergillus flavus allergenic extract 0.05 GM/ML Injectable Solution
  • RxCUI: 1006300 - Aspergillus niger var. niger allergenic extract 50 MG/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".