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  4. NDC Product Code: 12634-826 Benzonatate

NDC 12634-826 Benzonatate

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 12634-826?
  5. Benzonatate Uses
  6. Active Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
12634-826
Proprietary Name:
Benzonatate
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Apotheca Inc.
Labeler Code:
12634
Product Label ID:
271eabf9-0568-3974-e054-00144ff88e88
Start Marketing Date: [9]
06-04-2010
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330)
Shape:
OVAL (C48345)
Size(s):
9 MM
Imprint(s):
A1
Score:
1

Product Packages

NDC Code 12634-826-01

Package Description: 100 CAPSULE, LIQUID FILLED in 1 BOTTLE

NDC Code 12634-826-54

Package Description: 14 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Code 12634-826-61

Package Description: 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Code 12634-826-71

Package Description: 30 CAPSULE, LIQUID FILLED in 1 BOTTLE

NDC Code 12634-826-80

Package Description: 20 CAPSULE, LIQUID FILLED in 1 BOTTLE

NDC Code 12634-826-82

Package Description: 12 CAPSULE, LIQUID FILLED in 1 BOTTLE

NDC Code 12634-826-85

Package Description: 15 CAPSULE, LIQUID FILLED in 1 BOTTLE

NDC Code 12634-826-88

Package Description: 18 CAPSULE, LIQUID FILLED in 1 BOTTLE

NDC Code 12634-826-91

Package Description: 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Product Details

What is NDC 12634-826?

The NDC code 12634-826 is assigned by the FDA to the product Benzonatate which is product labeled by Apotheca Inc.. The product's dosage form is . The product is distributed in 9 packages with assigned NDC codes 12634-826-01 100 capsule, liquid filled in 1 bottle , 12634-826-54 14 capsule, liquid filled in 1 blister pack , 12634-826-61 10 capsule, liquid filled in 1 blister pack , 12634-826-71 30 capsule, liquid filled in 1 bottle , 12634-826-80 20 capsule, liquid filled in 1 bottle , 12634-826-82 12 capsule, liquid filled in 1 bottle , 12634-826-85 15 capsule, liquid filled in 1 bottle , 12634-826-88 18 capsule, liquid filled in 1 bottle , 12634-826-91 1 capsule, liquid filled in 1 blister 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 Benzonatate?

This medication is used to treat coughs caused by the common cold and other breathing problems (e.g., pneumonia, bronchitis, emphysema, asthma). It works by reducing the reflex in the lungs that causes the urge to cough. Use of this medication is not recommended in children younger than 10 years. Discuss the risks and benefits with your doctor.

Which are Benzonatate UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Benzonatate?

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 code indicates a single concept unique identifier (RXCUI) is associated with this product:

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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".