NDC 51672-2140 Terbinafine Hydrochloride

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:
51672-2140
Proprietary Name:
Terbinafine Hydrochloride
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Taro Pharmaceuticals U.s.a., Inc.
Labeler Code:
51672
Start Marketing Date: [9]
07-02-2007
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Product Packages

NDC Code 51672-2140-1

Package Description: 1 TUBE in 1 CARTON / 15 g in 1 TUBE

Product Details

What is NDC 51672-2140?

The NDC code 51672-2140 is assigned by the FDA to the product Terbinafine Hydrochloride which is product labeled by Taro Pharmaceuticals U.s.a., Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51672-2140-1 1 tube in 1 carton / 15 g in 1 tube. 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 Terbinafine Hydrochloride?

Adults and children 12 years and overuse the tip of the cap to break the seal and open the tubewash the affected skin with soap and water and dry completely before applyingfor athlete's foot wear well-fitting, ventilated shoes. Change shoes and socks at least once daily.between the toes only: apply twice a day (morning and night) for 1 week or as directed by a doctoron the bottom or sides of the foot: apply twice a day (morning and night) for 2 weeks or as directed by a doctorfor jock itch and ringworm: apply once a day (morning or night) for 1 week or as directed by a doctorwash hands after each usechildren under 12 years: ask a doctor1 week between the toes2 weeks on the bottom or sides of the foot

Which are Terbinafine Hydrochloride UNII Codes?

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

Which are Terbinafine 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 Terbinafine 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:

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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".