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  4. NDC Product Code: 65437-041 Acetaminophen And Diphenhydramine Hydrochloride

NDC 65437-041 Acetaminophen And Diphenhydramine Hydrochloride

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 65437-041?
  5. Acetaminophen And Diphenhydramine Hydrochloride Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. 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:
65437-041
Proprietary Name:
Acetaminophen And Diphenhydramine Hydrochloride
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Himprit Pharmachem Pvt Ltd
Labeler Code:
65437
Product Label ID:
6a2c1efb-d91b-48d2-b623-aa941e2c6f0e
Start Marketing Date: [9]
07-01-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
BLUE (C48333)
Shape:
OVAL (C48345)
Size(s):
18 MM
Score:
1

Code Structure Chart

Product Details

What is NDC 65437-041?

The NDC code 65437-041 is assigned by the FDA to the product Acetaminophen And Diphenhydramine Hydrochloride which is product labeled by Himprit Pharmachem Pvt Ltd. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 65437-041-31 1 bag in 1 drum / 31000 tablet, film coated in 1 bag, 65437-041-50 1 bag in 1 drum / 50000 tablet, film coated in 1 bag. 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 Acetaminophen And Diphenhydramine Hydrochloride?

This product is used as Active ingredients (in each Caplet)PurposeAcetaminophen 500 mgPain reliever/ fever reducerDiphenhydramine HCL 25 mgSleep Aid. Temporary relief of occasional headaches and minor aches and pain with accompanying sleeplessness

Which are Acetaminophen And Diphenhydramine Hydrochloride UNII Codes?

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

Which are Acetaminophen And Diphenhydramine Hydrochloride 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 Acetaminophen And Diphenhydramine Hydrochloride?

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:
  • RxCUI: 1092189 - acetaminophen 500 MG / diphenhydrAMINE HCl 25 MG Oral Tablet
  • RxCUI: 1092189 - acetaminophen 500 MG / diphenhydramine hydrochloride 25 MG Oral Tablet
  • RxCUI: 1092189 - APAP 500 MG / diphenhydramine hydrochloride 25 MG Oral Tablet

* 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".