NDC 36987-1075-1 Hog Epithelium

Package Information

What is NDC 36987-1075-1?

The NDC Code 36987-1075-1 is assigned to a package of 5 ml in 1 vial, multi-dose of Hog Epithelium, labeled by Nelco Laboratories, Inc.. The product's dosage form is and is administered via form. The following table has all the important details about this NDC code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

Field Name Field Value
NDC Code 36987-1075-1
Package Description 5 mL in 1 VIAL, MULTI-DOSE
Product Code 36987-1075
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.
Hog Epithelium
Usage Information Product Usage Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.
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.
11-Digit NDC Billing Format NDC Format for Billing
For insurance billing purposes the Centers for Medicare & Medicaid Services (CMS) created an 11 digit NDC derivative identifier. If the NDC Package code is less than 11 digits the code must be padded with leading zeros. The leading zeros must be added to the appropriate segment to create a 5-4-2 configuration.
NDC to RxNorm Crosswalk
  • RxCUI: 889656 - hog skin extract 20000 UNT/mL Injectable Solution
  • RxCUI: 889656 - hog skin extract 20000 UNT/ML Injectable Solution
  • RxCUI: 889656 - Sus scrofa skin extract 20,000 UNT/ML Injectable Solution
  • RxCUI: 894778 - duck feather extract 20,000 UNT/mL Injectable Solution
  • RxCUI: 894778 - duck feather extract 20000 UNT/ML Injectable Solution
  • Labeler Name Nelco Laboratories, Inc.
    Sample Package Sample Package?
    This field Indicates whether this package is a sample packaging or not.
    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.
    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.
    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".
    NDC Code Structure
    This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Other Product Packages

    The following packages are also available for Hog Epithelium with product NDC 36987-1075.

    NDC Package CodePackage Description
    36987-1075-210 mL in 1 VIAL, MULTI-DOSE
    36987-1075-330 mL in 1 VIAL, MULTI-DOSE
    36987-1075-450 mL in 1 VIAL, MULTI-DOSE

    * Please review the disclaimer below.