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  4. NDC Product Code: 0641-2965 Esmolol Hydrochloride

NDC 0641-2965 Esmolol Hydrochloride

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 0641-2965?
  4. Esmolol Hydrochloride Uses
  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:
0641-2965
Proprietary Name:
Esmolol Hydrochloride
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
West Ward Pharmaceutical Corporation
Labeler Code:
0641
Product Label ID:
a70baf53-e38a-4b23-8905-ee284170236d
Start Marketing Date: [9]
12-31-1986
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 0641-2965-45

Package Description: 25 VIAL in 1 BOX / 10 mL in 1 VIAL (0641-2965-41)

Product Details

What is NDC 0641-2965?

The NDC code 0641-2965 is assigned by the FDA to the product Esmolol Hydrochloride which is product labeled by West Ward Pharmaceutical Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0641-2965-45 25 vial in 1 box / 10 ml in 1 vial (0641-2965-41). 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 Esmolol Hydrochloride?

Esmolol hydrochloride is contraindicated in patients with sinus bradycardia, heart block greater than first degree, cardiogenic shock or overt heart failure (see WARNINGS).

Which are Esmolol Hydrochloride UNII Codes?

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

Which are Esmolol 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 Esmolol 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:

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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".