NDC 43857-0282 Strength F
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 43857-0282?
What are the uses for Strength F?
Which are Strength F UNII Codes?
The UNII codes for the active ingredients in this product are:
- .ALPHA.-KETOGLUTARIC ACID (UNII: 8ID597Z82X)
- .ALPHA.-KETOGLUTARIC ACID (UNII: 8ID597Z82X) (Active Moiety)
- ISOLEUCINE (UNII: 04Y7590D77)
- ISOLEUCINE (UNII: 04Y7590D77) (Active Moiety)
- ARGININE (UNII: 94ZLA3W45F)
- ARGININE (UNII: 94ZLA3W45F) (Active Moiety)
- LEVOCARNITINE (UNII: 0G389FZZ9M)
- LEVOCARNITINE (UNII: 0G389FZZ9M) (Active Moiety)
- LEUCINE (UNII: GMW67QNF9C)
- LEUCINE (UNII: GMW67QNF9C) (Active Moiety)
- ORNITHINE (UNII: E524N2IXA3)
- ORNITHINE (UNII: E524N2IXA3) (Active Moiety)
- VALINE (UNII: HG18B9YRS7)
- VALINE (UNII: HG18B9YRS7) (Active Moiety)
- ESTRADIOL (UNII: 4TI98Z838E)
- ESTRADIOL (UNII: 4TI98Z838E) (Active Moiety)
- ESTRONE (UNII: 2DI9HA706A)
- ESTRONE (UNII: 2DI9HA706A) (Active Moiety)
- PROGESTERONE (UNII: 4G7DS2Q64Y)
- PROGESTERONE (UNII: 4G7DS2Q64Y) (Active Moiety)
- TESTOSTERONE (UNII: 3XMK78S47O)
- TESTOSTERONE (UNII: 3XMK78S47O) (Active Moiety)
- ESTRIOL (UNII: FB33469R8E)
- ESTRIOL (UNII: FB33469R8E) (Active Moiety)
Which are Strength F 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
* 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".