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  4. NDC Product Code: 71335-0963 Chlorpheniramine Maleate 4 Mg

NDC 71335-0963 Chlorpheniramine Maleate 4 Mg

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 71335-0963?
  5. Chlorpheniramine Maleate 4 Mg 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:
71335-0963
Proprietary Name:
Chlorpheniramine Maleate 4 Mg
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bryant Ranch Prepack
Labeler Code:
71335
Product Label ID:
54681242-c861-4415-b5c0-d3ab55b62be1
Start Marketing Date: [9]
11-01-2015
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330)
Shape:
ROUND (C48348)
Size(s):
8 MM
Imprint(s):
AP;016
Score:
1

Code Structure Chart

Product Details

What is NDC 71335-0963?

The NDC code 71335-0963 is assigned by the FDA to the product Chlorpheniramine Maleate 4 Mg which is product labeled by Bryant Ranch Prepack. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 71335-0963-1 30 tablet in 1 bottle , 71335-0963-2 60 tablet in 1 bottle , 71335-0963-3 100 tablet in 1 bottle , 71335-0963-4 120 tablet in 1 bottle , 71335-0963-5 40 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 Chlorpheniramine Maleate 4 Mg?

Adults and children 12 years and overtake 1 tablet every 4 to 6 hours, not more than 6 tablets in 24 hourschildren 6 years to under 12 yearstake 1/2 tablet every 4 to 6 hours, not more than 3 tablets in 24 hourschildren under 6 yearsdo not use

Which are Chlorpheniramine Maleate 4 Mg UNII Codes?

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

Which are Chlorpheniramine Maleate 4 Mg 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 Chlorpheniramine Maleate 4 Mg?

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:

* Please review the disclaimer below.

Patient Education

Chlorpheniramine


Chlorpheniramine relieves red, itchy, watery eyes; sneezing; itchy nose or throat; and runny nose caused by allergies, hay fever, and the common cold. Chlorpheniramine helps control the symptoms of cold or allergies but will not treat the cause of the symptoms or speed recovery. Chlorpheniramine is in a class of medications called antihistamines. It works by blocking the action of histamine, a substance in the body that causes allergic symptoms.
[Learn More]


* 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".