NDC 61919-089 Xanax

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:
61919-089
Proprietary Name:
Xanax
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Direct Rx
Labeler Code:
61919
Start Marketing Date: [9]
06-02-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BLUE (C48333)
Shape:
OVAL (C48345)
Size(s):
9 MM
Imprint(s):
GG258
Score:
2

Product Packages

NDC Code 61919-089-30

Package Description: 30 TABLET in 1 BOTTLE

NDC Code 61919-089-60

Package Description: 60 TABLET in 1 BOTTLE

NDC Code 61919-089-90

Package Description: 90 TABLET in 1 BOTTLE

Product Details

What is NDC 61919-089?

The NDC code 61919-089 is assigned by the FDA to the product Xanax which is product labeled by Direct Rx. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 61919-089-30 30 tablet in 1 bottle , 61919-089-60 60 tablet in 1 bottle , 61919-089-90 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 Xanax?

Alprazolam is used to treat anxiety and panic disorders. It belongs to a class of medications called benzodiazepines which act on the brain and nerves (central nervous system) to produce a calming effect. It works by enhancing the effects of a certain natural chemical in the body (GABA).

Which are Xanax UNII Codes?

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

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Patient Education

Alprazolam


Alprazolam is used to treat anxiety disorders and panic disorder (sudden, unexpected attacks of extreme fear and worry about these attacks). Alprazolam is in a class of medications called benzodiazepines. It works by decreasing abnormal excitement 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".