NDC 49643-300 Alfalfa Pollen

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:
49643-300
Proprietary Name:
Alfalfa Pollen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Allermed Laboratories, Inc.
Labeler Code:
49643
Start Marketing Date: [9]
03-12-1974
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 49643-300-05

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

NDC Code 49643-300-10

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

NDC Code 49643-300-30

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

NDC Code 49643-300-50

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

Product Details

What is NDC 49643-300?

The NDC code 49643-300 is assigned by the FDA to the product Alfalfa Pollen 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 49643-300-05 5 ml in 1 vial, multi-dose , 49643-300-10 10 ml in 1 vial, multi-dose , 49643-300-30 30 ml in 1 vial, multi-dose , 49643-300-50 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 Alfalfa Pollen?

Allergenic extract may be used as a diagnostic skin test reagent in persons suspected of being sensitive to the allergenic source material from which the extract is made. Skin tests should be used in conjunction with a thorough allergic history to establish the relevance of a given allergen in the etiology of allergic disease. 4,5,6 Immunotherapy with allergenic extract is indicated in persons suffering from allergic rhinitis, bronchitis, conjunctivitis, urticaria and asthma. The therapeutic efficacy of allergenic extract has been proven in ragweed, grass, and mountain cedar pollinosis, cat-induced asthma and hypersensitivity to hymenoptera venoms. 7-12 Immunotherapy may be used along with or exclusive of antihistamines and other medications used to control allergic symptoms.

Which are Alfalfa Pollen UNII Codes?

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

  • ALNUS RHOMBIFOLIA POLLEN (UNII: 7X8HL8GRTM)
  • ALNUS RHOMBIFOLIA POLLEN (UNII: 7X8HL8GRTM) (Active Moiety)
  • MEDICAGO SATIVA POLLEN (UNII: G515RAI9FY)
  • MEDICAGO SATIVA POLLEN (UNII: G515RAI9FY) (Active Moiety)

Which are Alfalfa Pollen 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 Alfalfa Pollen?

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: 1011991 - Trichothecium roseum allergenic extract 100 MG/mL Injectable Solution
  • RxCUI: 1011991 - Trichothecium roseum allergenic extract 100 MG/ML Injectable Solution
  • RxCUI: 1011991 - Trichothecium roseum extract 0.1 GM/ML Injectable Solution
  • RxCUI: 1011991 - Trichothecium roseum extract 100 MG/ML Injectable Solution
  • RxCUI: 1115265 - bluegum eucalyptus pollen 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".