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  4. NDC Product Code: 55648-924 Enalapril Maleate

NDC 55648-924 Enalapril Maleate

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 55648-924?
  5. Enalapril Maleate 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:
55648-924
Proprietary Name:
Enalapril Maleate
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Wockhardt Limited
Labeler Code:
55648
Product Label ID:
f1ec6ac1-6b94-40bb-a329-9056f201090c
Start Marketing Date: [9]
12-11-2009
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - WHITE)
Shape:
ROUND (C48348)
Size(s):
6 MM
8 MM
Imprint(s):
W;923
W;924
Score:
2

Product Packages

NDC Code 55648-924-01

Package Description: 90 TABLET in 1 BOTTLE

NDC Code 55648-924-02

Package Description: 100 TABLET in 1 BOTTLE

NDC Code 55648-924-03

Package Description: 1000 TABLET in 1 BOTTLE

NDC Code 55648-924-07

Package Description: 10 BLISTER PACK in 1 CARTON / 10 TABLET in 1 BLISTER PACK

NDC Code 55648-924-09

Package Description: 40000 TABLET in 1 DRUM

NDC Code 55648-924-10

Package Description: 8000 TABLET in 1 DRUM

Product Details

What is NDC 55648-924?

The NDC code 55648-924 is assigned by the FDA to the product Enalapril Maleate which is product labeled by Wockhardt Limited. The product's dosage form is . The product is distributed in 6 packages with assigned NDC codes 55648-924-01 90 tablet in 1 bottle , 55648-924-02 100 tablet in 1 bottle , 55648-924-03 1000 tablet in 1 bottle , 55648-924-07 10 blister pack in 1 carton / 10 tablet in 1 blister pack, 55648-924-09 40000 tablet in 1 drum , 55648-924-10 8000 tablet in 1 drum . 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 Enalapril Maleate?

Enalapril is used to treat high blood pressure. Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems. It is also used to treat heart failure and to help prevent people with a certain heart problem (left ventricular dysfunction) from developing heart failure. Enalapril belongs to a class of drugs known as ACE inhibitors. It works by relaxing blood vessels so blood can flow more easily.

Which are Enalapril Maleate UNII Codes?

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

Which are Enalapril Maleate 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 Enalapril Maleate?

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:

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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".