NDC 51672-2140 Terbinafine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51672 - Taro Pharmaceuticals U.s.a., Inc.
- 51672-2140 - Terbinafine Hydrochloride
Product Characteristics
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?
What are the uses for Terbinafine Hydrochloride?
Which are Terbinafine Hydrochloride 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 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:
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- WATER (UNII: 059QF0KO0R)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
What is the NDC to RxNorm Crosswalk for Terbinafine Hydrochloride?
- RxCUI: 992528 - terbinafine HCl 1 % Topical Cream
- RxCUI: 992528 - terbinafine hydrochloride 10 MG/ML Topical Cream
- RxCUI: 992528 - terbinafine hydrochloride 1 % Topical Cream
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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".