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  4. NDC Product Code: 61919-088 Diazepam

NDC 61919-088 Diazepam

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 61919-088?
  5. Diazepam Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk
  9. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
61919-088
Proprietary Name:
Diazepam
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Direct Rx
Labeler Code:
61919
Product Label ID:
8d573383-ff68-5771-e053-2a95a90acdf4
Start Marketing Date: [9]
03-07-2017
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330)
Shape:
ROUND (C48348)
Size(s):
8 MM
Imprint(s):
DAN;5619;5
Score:
2

Product Packages

NDC Code 61919-088-02

Package Description: 2 TABLET in 1 BOTTLE

NDC Code 61919-088-03

Package Description: 3 TABLET in 1 BOTTLE

NDC Code 61919-088-30

Package Description: 30 TABLET in 1 BOTTLE

NDC Code 61919-088-60

Package Description: 60 TABLET in 1 BOTTLE

NDC Code 61919-088-72

Package Description: 120 TABLET in 1 BOTTLE

NDC Code 61919-088-90

Package Description: 90 TABLET in 1 BOTTLE

Product Details

What is NDC 61919-088?

The NDC code 61919-088 is assigned by the FDA to the product Diazepam which is product labeled by Direct Rx. The product's dosage form is . The product is distributed in 6 packages with assigned NDC codes 61919-088-02 2 tablet in 1 bottle , 61919-088-03 3 tablet in 1 bottle , 61919-088-30 30 tablet in 1 bottle , 61919-088-60 60 tablet in 1 bottle , 61919-088-72 120 tablet in 1 bottle , 61919-088-90 90 tablet in 1 bottle . 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 Diazepam?

Diazepam is used to treat anxiety, alcohol withdrawal, and seizures. It is also used to relieve muscle spasms and to provide sedation before medical procedures. This medication works by calming the brain and nerves. Diazepam belongs to a class of drugs known as benzodiazepines.

Which are Diazepam UNII Codes?

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

Which are Diazepam 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 Diazepam?

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:

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Patient Education

Diazepam


Diazepam is used to relieve anxiety and to control agitation caused by alcohol withdrawal. It is also used along with other medications to control muscle spasms and spasticity caused by certain neurological disorders such as cerebral palsy (condition that causes difficulty with movement and balance), paraplegia (inability to move parts of the body), athetosis (abnormal muscle contractions), and stiff-man syndrome (a rare disorder with muscle rigidity and stiffness). Diazepam is also used along with other medications to control seizures. Diazepam is in a class of medications called benzodiazepines. It works by calming abnormal overactivity in the brain.
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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".