NDC 10530-319 Nexavir

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:
10530-319
Proprietary Name:
Nexavir
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nexco Pharma
Labeler Code:
10530
Start Marketing Date: [9]
02-19-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BROWN (C48332 - BROWN SOLUTION)

Product Packages

NDC Code 10530-319-07

Package Description: 20 mL in 1 VIAL, MULTI-DOSE

Product Details

What is NDC 10530-319?

The NDC code 10530-319 is assigned by the FDA to the product Nexavir which is product labeled by Nexco Pharma. The product's dosage form is . The product is distributed in a single package with assigned NDC code 10530-319-07 20 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 Nexavir?

A wide range of dermatological clinical conditions benefit from NEXAVIR ® therapy. The common denominator in these varied conditions is the presence of inflammation and edema. Favourable responses to the administration of NEXAVIR ® in patients with acne vulgaris 5,6,7,8, herpes zoster, "poison ivy" dermatitis, pityriasis rosea, seborrheic dermatitis, urticaria and eczema 9,10,11, severe sunburn 12 and rosacea 13 have been reported.

Which are Nexavir UNII Codes?

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

Which are Nexavir 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 Nexavir?

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: 200238 - liver derivative complex 25.5 MG/ML Injectable Solution
  • RxCUI: 880859 - Nexavir 25.5 MG/ML Injectable Solution
  • RxCUI: 880859 - liver derivative complex 25.5 MG/ML Injectable Solution [Nexavir]

* Please review the disclaimer below.

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".