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  4. NDC Product Code: 62756-329 Epinastine Hydrochloride

NDC 62756-329 Epinastine Hydrochloride

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 62756-329?
  4. Epinastine Hydrochloride Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk
  8. 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:
62756-329
Proprietary Name:
Epinastine Hydrochloride
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Sun Pharmaceutical Industries, Inc.
Labeler Code:
62756
Product Label ID:
cafe4650-6aa4-4466-9beb-064ee5a0e401
Start Marketing Date: [9]
11-01-2011
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 62756-329-90

Package Description: 1 BOTTLE in 1 CARTON / 5 mL in 1 BOTTLE

Price per Unit: $14.50175 per ML

Product Details

What is NDC 62756-329?

The NDC code 62756-329 is assigned by the FDA to the product Epinastine Hydrochloride which is product labeled by Sun Pharmaceutical Industries, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 62756-329-90 1 bottle in 1 carton / 5 ml 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 Epinastine Hydrochloride?

Epinastine hydrochloride ophthalmic solution is indicated for the prevention of itching associated with allergic conjunctivitis.

Which are Epinastine Hydrochloride UNII Codes?

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

Which are Epinastine 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 Epinastine 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: 860654 - epinastine HCl 0.05 % Ophthalmic Solution
  • RxCUI: 860654 - epinastine hydrochloride 0.5 MG/ML Ophthalmic Solution
  • RxCUI: 860654 - epinastine hydrochloride 0.05 % (as epinastine 0.044 % ) Ophthalmic Solution
  • RxCUI: 860654 - epinastine hydrochloride 0.05 % Ophthalmic Solution

* Please review the disclaimer below.

Patient Education

Epinastine Ophthalmic


Ophthalmic epinastine is used to prevent itching of the eyes caused by allergic conjunctivitis (a condition in which the eyes become itchy, swollen, red, and teary when they are exposed to certain substances in the air). Epinastine is in a class of medications called antihistamines. It works by preventing the release of natural substances which cause allergic reactions in the eyes.
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* 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".