NDC 54868-6425 Zenatane
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 54868-6425?
What are the uses for Zenatane?
Which are Zenatane UNII Codes?
The UNII codes for the active ingredients in this product are:
- ISOTRETINOIN (UNII: EH28UP18IF)
- ISOTRETINOIN (UNII: EH28UP18IF) (Active Moiety)
Which are Zenatane 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:
- BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- HYDROGENATED SOYBEAN OIL (UNII: A2M91M918C)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- SOYBEAN OIL (UNII: 241ATL177A)
- WHITE WAX (UNII: 7G1J5DA97F)
- GELATIN (UNII: 2G86QN327L)
- GLYCERIN (UNII: PDC6A3C0OX)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- D&C RED NO. 27 (UNII: 2LRS185U6K)
- D&C RED NO. 30 (UNII: 2S42T2808B)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- BUTYL ALCOHOL (UNII: 8PJ61P6TS3)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SHELLAC (UNII: 46N107B71O)
What is the NDC to RxNorm Crosswalk for Zenatane?
- RxCUI: 1373335 - ZENATANE 20 MG Oral Capsule
- RxCUI: 1373335 - isotretinoin 20 MG Oral Capsule [Zenatane]
- RxCUI: 1373335 - Zenatane 20 MG Oral Capsule
- RxCUI: 1373337 - ZENATANE 40 MG Oral Capsule
- RxCUI: 1373337 - isotretinoin 40 MG Oral Capsule [Zenatane]
* Please review the disclaimer below.
[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".