1. Home
  2. Labeler Index
  3. Avera Mckennan Hospital
  4. NDC Product Code: 69189-4246 Lorazepam

NDC 69189-4246 Lorazepam

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 69189-4246?
  5. Lorazepam Uses
  6. Active Ingredients UNII Codes
  7. 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:
69189-4246
Proprietary Name:
Lorazepam
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Avera Mckennan Hospital
Labeler Code:
69189
Product Label ID:
e4a0c2f1-ec45-438d-b2e3-fa61915ca8f6
Start Marketing Date: [9]
05-01-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
6 MM
Imprint(s):
4007;V
Score:
1

Code Structure Chart

Product Details

What is NDC 69189-4246?

The NDC code 69189-4246 is assigned by the FDA to the product Lorazepam which is product labeled by Avera Mckennan Hospital. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 69189-4246-1 1 tablet in 1 dose pack , 69189-4246-5 .5 tablet in 1 dose pack . 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 Lorazepam?

This medication is used to treat anxiety. Lorazepam belongs to a class of drugs known as benzodiazepines which act on the brain and nerves (central nervous system) to produce a calming effect. This drug works by enhancing the effects of a certain natural chemical in the body (GABA).

Which are Lorazepam UNII Codes?

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

Which are Lorazepam 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".