NDC 65044-3141 Food - Plant Source, Celery Apium Graveolens

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:
65044-3141
Proprietary Name:
Food - Plant Source, Celery Apium Graveolens
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jubilant Hollisterstier Llc
Labeler Code:
65044
Start Marketing Date: [9]
04-19-1941
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 65044-3141-1

Package Description: 5 mL in 1 VIAL

Product Details

What is NDC 65044-3141?

The NDC code 65044-3141 is assigned by the FDA to the product Food - Plant Source, Celery Apium Graveolens which is product labeled by Jubilant Hollisterstier Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 65044-3141-1 5 ml in 1 vial . 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 Food - Plant Source, Celery Apium Graveolens?

Certain diagnostics carry labeling which states Allergenic Extract for Diagnostic Use Only. Data to support the therapeutic use of products labeled with this statement have not been established. 14In addition to a carefully taken history, the use of glycerin-containing extracts in scratch, prick or puncture testing is an accepted method in the diagnosis of allergic conditions. 1, 2, 3 Extracts of all allergens do not produce equivalent results in scratch, prick or puncture tests. The intensity of the skin reactions produced will be determined by two factors: the degree of sensitivity of the patient, and the nature of the allergenic extract applied. Scratch, prick or puncture tests are not as sensitive as the intradermal test, but are safer and cause less discomfort. They may, therefore, be the method of choice when a large number of tests are needed, or when testing the pediatric patient. In some cases, where the relatively insensitive scratch, prick or puncture tests are negative or do not confirm the allergic history, follow-up intradermal tests may be positive. However, ANTIGENS PRODUCING LARGE 3 to 4+ SCRATCH, PRICK OR PUNCTURE TESTS SHOULD NOT BE TESTED INTRADERMALLY.

Which are Food - Plant Source, Celery Apium Graveolens UNII Codes?

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

Which are Food - Plant Source, Celery Apium Graveolens 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 Food - Plant Source, Celery Apium Graveolens?

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: 891657 - brazil nut allergenic extract 100 MG/ML Injectable Solution
  • RxCUI: 891657 - brazil nut allergenic extract 0.1 GM/ML Injectable Solution
  • RxCUI: 891774 - apple allergenic extract 100 MG/ML Injectable Solution
  • RxCUI: 891774 - apple allergenic extract 0.1 GM/ML Injectable Solution
  • RxCUI: 891833 - banana allergenic extract 100 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".