NDC 63629-2953 Lorazepam

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:
63629-2953
Proprietary Name:
Lorazepam
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bryant Ranch Prepack
Labeler Code:
63629
Start Marketing Date: [9]
10-31-1991
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
6 MM
Imprint(s):
240;0;5;WATSON
Score:
2

Product Packages

NDC Code 63629-2953-1

Package Description: 30 TABLET in 1 BOTTLE

NDC Code 63629-2953-2

Package Description: 10 TABLET in 1 BOTTLE

NDC Code 63629-2953-3

Package Description: 60 TABLET in 1 BOTTLE

NDC Code 63629-2953-4

Package Description: 90 TABLET in 1 BOTTLE

NDC Code 63629-2953-5

Package Description: 15 TABLET in 1 BOTTLE

NDC Code 63629-2953-6

Package Description: 100 TABLET in 1 BOTTLE

NDC Code 63629-2953-7

Package Description: 120 TABLET in 1 BOTTLE

NDC Code 63629-2953-8

Package Description: 2 TABLET in 1 BOTTLE

NDC Code 63629-2953-9

Package Description: 5 TABLET in 1 BOTTLE

Product Details

What is NDC 63629-2953?

The NDC code 63629-2953 is assigned by the FDA to the product Lorazepam which is product labeled by Bryant Ranch Prepack. The product's dosage form is . The product is distributed in 9 packages with assigned NDC codes 63629-2953-1 30 tablet in 1 bottle , 63629-2953-2 10 tablet in 1 bottle , 63629-2953-3 60 tablet in 1 bottle , 63629-2953-4 90 tablet in 1 bottle , 63629-2953-5 15 tablet in 1 bottle , 63629-2953-6 100 tablet in 1 bottle , 63629-2953-7 120 tablet in 1 bottle , 63629-2953-8 2 tablet in 1 bottle , 63629-2953-9 5 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 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:

What is the NDC to RxNorm Crosswalk for Lorazepam?

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:

* Please review the disclaimer below.

Patient Education

Lorazepam


Lorazepam is used to relieve anxiety. Lorazepam is also used to treat insomnia caused by anxiety or temporary situational stress. Lorazepam is in a class of medications called benzodiazepines. It works by slowing activity in the brain to allow for relaxation.
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* 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".