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  4. NDC Product Code: 54868-5905 Famciclovir

NDC 54868-5905 Famciclovir

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 54868-5905?
  5. Famciclovir Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. 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:
54868-5905
Proprietary Name:
Famciclovir
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Physicians Total Care, Inc.
Labeler Code:
54868
Product Label ID:
405372a1-83bc-4843-b1b2-bd8ff2f83f87
Start Marketing Date: [9]
06-16-2008
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
OVAL (C48345)
Size(s):
18 MM
Imprint(s):
8119;93
Score:
1

Product Packages

NDC Code 54868-5905-0

Package Description: 20 TABLET, FILM COATED in 1 BOTTLE

NDC Code 54868-5905-1

Package Description: 21 TABLET, FILM COATED in 1 BOTTLE

NDC Code 54868-5905-2

Package Description: 3 TABLET, FILM COATED in 1 BOTTLE

NDC Code 54868-5905-3

Package Description: 10 TABLET, FILM COATED in 1 BOTTLE

NDC Code 54868-5905-4

Package Description: 30 TABLET, FILM COATED in 1 BOTTLE

Product Details

What is NDC 54868-5905?

The NDC code 54868-5905 is assigned by the FDA to the product Famciclovir which is product labeled by Physicians Total Care, Inc.. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 54868-5905-0 20 tablet, film coated in 1 bottle , 54868-5905-1 21 tablet, film coated in 1 bottle , 54868-5905-2 3 tablet, film coated in 1 bottle , 54868-5905-3 10 tablet, film coated in 1 bottle , 54868-5905-4 30 tablet, film coated 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 Famciclovir?

Famciclovir is used to treat infections caused by certain types of viruses. It treats shingles caused by herpes zoster. It also treats outbreaks of herpes simplex that cause cold sores around the mouth, sores around the anus, and genital herpes. In people with frequent outbreaks of genital herpes, famciclovir is used to help reduce the number of future episodes. Famciclovir is an antiviral drug. However, it is not a cure for these infections. The viruses that cause these infections continue to live in the body even between outbreaks. Famciclovir decreases the severity and length of these outbreaks. It helps the sores heal faster, keeps new sores from forming, and decreases pain/itching. This medication may also help reduce how long pain remains after the sores heal. In addition, in people with a weakened immune system, famciclovir can decrease the risk of the virus spreading to other parts of the body and causing serious infections.

Which are Famciclovir UNII Codes?

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

Which are Famciclovir 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 Famciclovir?

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:

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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".