NDC 71335-1124 Terbinafine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Product Packages
NDC Code 71335-1124-1
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 71335-1124-2
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 71335-1124-3
Package Description: 90 TABLET in 1 BOTTLE
NDC Code 71335-1124-4
Package Description: 100 TABLET in 1 BOTTLE
NDC Code 71335-1124-5
Package Description: 7 TABLET in 1 BOTTLE
NDC Code 71335-1124-6
Package Description: 40 TABLET in 1 BOTTLE
NDC Code 71335-1124-7
Package Description: 45 TABLET in 1 BOTTLE
NDC Code 71335-1124-8
Package Description: 14 TABLET in 1 BOTTLE
NDC Code 71335-1124-9
Package Description: 28 TABLET in 1 BOTTLE
Product Details
What is NDC 71335-1124?
What are the uses for Terbinafine?
Which are Terbinafine UNII Codes?
The UNII codes for the active ingredients in this product are:
- TERBINAFINE HYDROCHLORIDE (UNII: 012C11ZU6G)
- TERBINAFINE (UNII: G7RIW8S0XP) (Active Moiety)
Which are Terbinafine 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:
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- HYPROMELLOSE 2910 (5 MPA.S) (UNII: R75537T0T4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
What is the NDC to RxNorm Crosswalk for Terbinafine?
- RxCUI: 313222 - terbinafine HCl 250 MG Oral Tablet
- RxCUI: 313222 - terbinafine 250 MG Oral Tablet
- RxCUI: 313222 - terbinafine (as terbinafine HCl) 250 MG Oral Tablet
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Patient Education
Terbinafine
Terbinafine granules are used to treat fungal infections of the scalp. Terbinafine tablets are used to treat fungal infections of the toenails and fingernails. Terbinafine is in a class of medications called antifungals. It works by stopping the growth of fungi.
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[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".