NDC 71335-1092 Alprazolam

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:
71335-1092
Proprietary Name:
Alprazolam
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bryant Ranch Prepack
Labeler Code:
71335
Start Marketing Date: [9]
07-09-2018
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
ORANGE (C48331 - LIGHT ORANGE TO ORANGE)
Shape:
OVAL (C48345)
Size(s):
9 MM
Imprint(s):
B705
Score:
2

Product Packages

NDC Code 71335-1092-0

Package Description: 10 TABLET in 1 BOTTLE

NDC Code 71335-1092-1

Package Description: 15 TABLET in 1 BOTTLE

NDC Code 71335-1092-2

Package Description: 30 TABLET in 1 BOTTLE

NDC Code 71335-1092-3

Package Description: 20 TABLET in 1 BOTTLE

NDC Code 71335-1092-4

Package Description: 100 TABLET in 1 BOTTLE

NDC Code 71335-1092-5

Package Description: 90 TABLET in 1 BOTTLE

NDC Code 71335-1092-6

Package Description: 60 TABLET in 1 BOTTLE

NDC Code 71335-1092-7

Package Description: 120 TABLET in 1 BOTTLE

NDC Code 71335-1092-8

Package Description: 28 TABLET in 1 BOTTLE

NDC Code 71335-1092-9

Package Description: 2 TABLET in 1 BOTTLE

Product Details

What is NDC 71335-1092?

The NDC code 71335-1092 is assigned by the FDA to the product Alprazolam which is product labeled by Bryant Ranch Prepack. The product's dosage form is . The product is distributed in 10 packages with assigned NDC codes 71335-1092-0 10 tablet in 1 bottle , 71335-1092-1 15 tablet in 1 bottle , 71335-1092-2 30 tablet in 1 bottle , 71335-1092-3 20 tablet in 1 bottle , 71335-1092-4 100 tablet in 1 bottle , 71335-1092-5 90 tablet in 1 bottle , 71335-1092-6 60 tablet in 1 bottle , 71335-1092-7 120 tablet in 1 bottle , 71335-1092-8 28 tablet in 1 bottle , 71335-1092-9 2 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 Alprazolam?

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 Alprazolam UNII Codes?

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

Which are Alprazolam 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 Alprazolam?

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

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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* 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".