NDC 75834-101 Psoriatar (coal Tar)

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:
75834-101
Proprietary Name:
Psoriatar (coal Tar)
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nivagen Pharmaceuticals, Inc.
Labeler Code:
75834
Start Marketing Date: [9]
05-15-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 75834-101-01

Package Description: 1 CAN in 1 CARTON / 100 g in 1 CAN

Product Details

What is NDC 75834-101?

The NDC code 75834-101 is assigned by the FDA to the product Psoriatar (coal Tar) which is product labeled by Nivagen Pharmaceuticals, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 75834-101-01 1 can in 1 carton / 100 g in 1 can. 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 Psoriatar (coal Tar)?

Shake the can before use.Invert the can to dispense. Upright dispensing will cause loss of propellant.Apply to affected areas one to four times daily or as directed by a doctor.

Which are Psoriatar (coal Tar) UNII Codes?

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

Which are Psoriatar (coal Tar) 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 Psoriatar (coal Tar)?

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".