NDC 36987-1269 Sword Fish

Table of Contents

    1. Product Information
    2. Product Packages
    3. What is NDC 36987-1269?
    4. Sword Fish Uses
    5. Active Ingredients UNII Codes
    6. Inactive Ingredients UNII Codes
    7. NDC to RxNorm Crosswalk

Product Information

NDC Product Code36987-1269
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.		Sword Fish
NDC Directory StatusINACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.		Nelco Laboratories, Inc.
Labeler Code36987
SPL SET ID:026f2f1e-71cf-47ab-a24d-66663ff98429
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.		08-29-1972
Listing Expiration Date 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.		12-31-2017
Exclude Flag 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". 		I
NDC Code Structure

Product Packages

NDC Code 36987-1269-1

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

NDC Code 36987-1269-2

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

NDC Code 36987-1269-3

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

NDC Code 36987-1269-4

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

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Product Details

What is NDC 36987-1269?

The NDC code 36987-1269 is assigned by the FDA to the product Sword Fish which is product labeled by Nelco Laboratories, Inc.. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 36987-1269-1 5 ml in 1 vial, multi-dose , 36987-1269-2 10 ml in 1 vial, multi-dose , 36987-1269-3 30 ml in 1 vial, multi-dose , 36987-1269-4 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 Sword Fish?

Allergenic extracts are indicated for use in diagnostic testing and as part of a treatment regime for allergic disease, as established by allergy history and skin test reactivity. Allergenic extracts are indicated for the treatment of allergen specific allergic disease for use as hyposensitization or immunotherapy when avoidance of specific allergens can not be attained. The use of allergenic extracts for therapeutic purpose has been established by well-controlled clinical studies. Allergenic extracts may be used as adjunctive therapy along with pharmacotherapy which includes antihistamines, corticosteroids, and cromoglycate, and avoidance measures. Allergenic extracts for therapeutic use should be given using only the allergen selection to which the patient is allergic, has a history of exposure and are likely to be exposed to again.

Which are Sword Fish UNII Codes?

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

Which are Sword Fish 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 Sword Fish?

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: 892506 - tuna allergenic extract 100 MG/ML Injectable Solution
  • RxCUI: 892506 - tuna allergenic extract 0.1 GM/ML Injectable Solution
  • RxCUI: 892542 - clam allergenic extract 100 MG/ML Injectable Solution
  • RxCUI: 892542 - quahog allergenic extract 0.1 GM/ML Injectable Solution
  • RxCUI: 892546 - codfish allergenic extract 100 MG/ML Injectable Solution

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