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  4. NDC Product Code: 73028-401 Hydrocortisone Acetate Pramoxine Hydrochloride

NDC 73028-401 Hydrocortisone Acetate Pramoxine Hydrochloride

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 73028-401?
  5. Hydrocortisone Acetate Pramoxine Hydrochloride Uses
  6. Active 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:
73028-401
Proprietary Name:
Hydrocortisone Acetate Pramoxine Hydrochloride
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Pageview Pharmaceuticals
Labeler Code:
73028
Product Label ID:
ac9617e7-0487-4ec8-8714-edcf967e9e50
Start Marketing Date: [9]
01-24-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Code Structure Chart

Product Details

What is NDC 73028-401?

The NDC code 73028-401 is assigned by the FDA to the product Hydrocortisone Acetate Pramoxine Hydrochloride which is product labeled by Pageview Pharmaceuticals. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73028-401-12 2 blister pack in 1 box / 6 suppository in 1 blister pack (73028-401-01). 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 Hydrocortisone Acetate Pramoxine Hydrochloride?

Hydrocortisone acetate and pramoxine hydrochloride suppositories are indicated for use in inflamed hemorrhoids, post-irradiation (factitial) proctitis; as an adjunct in the treatment of chronic ulcerative colitis; cryptitis; and other inflammatory conditions of anorectum and pruritus ani.

Which are Hydrocortisone Acetate Pramoxine Hydrochloride UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Hydrocortisone Acetate Pramoxine 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 code indicates a single concept unique identifier (RXCUI) is associated with this product:
  • RxCUI: 2590741 - hydrocortisone acetate 25 MG / pramoxine hydrochloride 18 MG Rectal Suppository

* 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".