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  4. NDC Product Code: 48951-5033 Hypophysis 6

NDC 48951-5033 Hypophysis 6

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 48951-5033?
  4. Hypophysis 6 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:
48951-5033
Proprietary Name:
Hypophysis 6
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Uriel Pharmacy Inc.
Labeler Code:
48951
Product Label ID:
862b8a06-5b07-4039-97bf-6d91553d6da0
Start Marketing Date: [9]
09-01-2009
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 48951-5033?

The NDC code 48951-5033 is assigned by the FDA to the product Hypophysis 6 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 48951-5033-1 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 Hypophysis 6?

Directions: FOR ORAL USE.

Which are Hypophysis 6 UNII Codes?

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

  • BOS TAURUS PITUITARY GLAND (UNII: 7JM57I419K)
  • BOS TAURUS PITUITARY GLAND (UNII: 7JM57I419K) (Active Moiety)

Which are Hypophysis 6 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".