NDC 0485-0210 Ed-a-hist Pse

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
0485-0210
Proprietary Name:
Ed-a-hist Pse
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
0485
Start Marketing Date: [9]
10-08-2011
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329)
Shape:
OVAL (C48345)
Size(s):
13 MM
Imprint(s):
ED;PSE
Score:
2

Code Structure Chart

Product Details

What is NDC 0485-0210?

The NDC code 0485-0210 is assigned by the FDA to the product Ed-a-hist Pse which is product labeled by Edwards Pharmaceuticals, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0485-0210-01 100 tablet, coated in 1 bottle, plastic . 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 Ed-a-hist Pse?

Do not exceed recommended dosage.Adults and children 12 years of age and over:1 tablet every 4-6 hours, not to exceed 4 tablets in 24 hours, or as directed by a doctorChildren 6 to under 12 years of age:1/2 tablet every 4-6 hours, not to exceed 2 tablets in 24 hours, or as directed by a doctorChildren under 6 years of age:Consult a doctor.

Which are Ed-a-hist Pse UNII Codes?

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

Which are Ed-a-hist Pse 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 Ed-a-hist Pse?

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: 1099446 - pseudoephedrine HCl 60 MG / triprolidine HCl 2.5 MG Oral Tablet
  • RxCUI: 1099446 - pseudoephedrine hydrochloride 60 MG / triprolidine hydrochloride 2.5 MG Oral Tablet

* 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".