1. Home
  2. Labeler Index
  3. Wockhardt Limited
  4. NDC Product Code: 55648-312 Donepezil Hydrochloride

NDC 55648-312 Donepezil Hydrochloride

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 55648-312?
  5. Active Ingredients UNII Codes
  6. Inactive 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:
55648-312
Proprietary Name:
Donepezil Hydrochloride
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Wockhardt Limited
Labeler Code:
55648
Product Label ID:
b7c926f0-8771-41d7-95be-3d4110dc0603
Start Marketing Date: [9]
05-28-2011
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - WHITE)
YELLOW (C48330 - YELLOW)
Shape:
ROUND (C48348)
Size(s):
7 MM
9 MM
Imprint(s):
W;311
W;312
Score:
1

Code Structure Chart

Product Details

What is NDC 55648-312?

The NDC code 55648-312 is assigned by the FDA to the product Donepezil Hydrochloride which is product labeled by Wockhardt Limited. The product's dosage form is . The product is distributed in 8 packages with assigned NDC codes 55648-312-01 30 tablet, film coated in 1 bottle , 55648-312-02 60 tablet, film coated in 1 bottle , 55648-312-03 90 tablet, film coated in 1 bottle , 55648-312-04 500 tablet, film coated in 1 bottle , 55648-312-05 1000 tablet, film coated in 1 bottle , 55648-312-06 100 blister pack in 1 carton / 1 tablet, film coated in 1 blister pack, 55648-312-07 28 tablet, film coated in 1 bottle , 55648-312-08 100 tablet, film coated 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.

Which are Donepezil Hydrochloride UNII Codes?

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

Which are Donepezil 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 Donepezil 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:

* 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".