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  4. NDC Product Code: 48951-9080 Viscum (i) Mali Series 0

NDC 48951-9080 Viscum (i) Mali Series 0

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 48951-9080?
  4. Viscum (i) Mali Series 0 Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
48951-9080
Proprietary Name:
Viscum (i) Mali Series 0
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Uriel Pharmacy Inc.
Labeler Code:
48951
Product Label ID:
14d73d09-be94-4c43-b5db-3bda5c2a7682
Start Marketing Date: [9]
09-01-2009
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 48951-9080-1

Package Description: 10 AMPULE in 1 BOX / 1 mL in 1 AMPULE

Product Details

What is NDC 48951-9080?

The NDC code 48951-9080 is assigned by the FDA to the product Viscum (i) Mali Series 0 which is product labeled by Uriel Pharmacy Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 48951-9080-1 10 ampule in 1 box / 1 ml in 1 ampule. 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 Viscum (i) Mali Series 0?

Directions: FOR ORAL USE.

Which are Viscum (i) Mali Series 0 UNII Codes?

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

  • VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP)
  • VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP) (Active Moiety)

Which are Viscum (i) Mali Series 0 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:

* 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".